Cambrex Corporation
NDC Database

Cambrex Corporation

NDC Database

National Drug Code (NDC) records including drug products, NDC numbers, nonproprietary names, dosage forms, strengths, labelers and marketing information.

Bulk Ingredient
  • Total Records 168
  • Latest Marketing Date 2023-10-31
  • Data Source FDA
  • First Marketing Date 1986-01-21
Company Overview

Company

Cambrex Corporation

Country

U.S.A

Social Profiles

LinkedIn X / Twitter
Company Snapshot

Cambrex Corporation

One Meadowlands Plaza, East Rutherford, NJ 07073

U.S.A

www.cambrex.com/ info@cambrex.com View on Map
NDC Records ( 168 records )
2012
26 Oct
Bulk Ingredient NDC: 59116-0630

Nonproprietary Name

Sulfasalazine

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-0630

Substance

SULFASALAZINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-10-26

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2012
26 Oct
Bulk Ingredient NDC: 59116-0631

Nonproprietary Name

Sulfasalazine

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-0631

Substance

SULFASALAZINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-10-26

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2012
26 Oct
Bulk Ingredient NDC: 59116-0632

Nonproprietary Name

Sulfasalazine

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-0632

Substance

SULFASALAZINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-10-26

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2012
26 Oct
Bulk Ingredient NDC: 59116-0633

Nonproprietary Name

Sulfasalazine

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-0633

Substance

SULFASALAZINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-10-26

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2012
26 Oct
Bulk Ingredient NDC: 59116-1800

Nonproprietary Name

Nicotine Polacrilex

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-1800

Substance

NICOTINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-10-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
26 Oct
Bulk Ingredient NDC: 59116-1801

Nonproprietary Name

Nicotine Resinate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-1801

Substance

NICOTINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-10-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2016
26 Apr
Bulk Ingredient NDC: 59116-1803

Nonproprietary Name

Nicotine Polacrilex

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-1803

Substance

NICOTINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2016-04-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2017
03 Apr
Bulk Ingredient NDC: 59116-1804

Nonproprietary Name

Nicotine Resinate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-1804

Substance

NICOTINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2017-04-03

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
26 Oct
Bulk Ingredient NDC: 59116-1820

Nonproprietary Name

Ofloxacin

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-1820

Substance

OFLOXACIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-10-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
26 Oct
Bulk Ingredient NDC: 59116-1850

Nonproprietary Name

Ondansetron Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-1850

Substance

ONDANSETRON HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-10-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
26 Oct
Bulk Ingredient NDC: 59116-1851

Nonproprietary Name

Ondansetron Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-1851

Substance

ONDANSETRON HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-10-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
26 Oct
Bulk Ingredient NDC: 59116-1852

Nonproprietary Name

Ondansetron Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-1852

Substance

ONDANSETRON HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-10-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
26 Oct
Bulk Ingredient NDC: 59116-1853

Nonproprietary Name

Ondansetron Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-1853

Substance

ONDANSETRON HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-10-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
26 Oct
Bulk Ingredient NDC: 59116-1930

Nonproprietary Name

Phenyl-2-(S)-Aminopropane Saccharate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-1930

Substance

DEXTROAMPHETAMINE SACCHARATE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2012-10-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
26 Oct
Bulk Ingredient NDC: 59116-1931

Nonproprietary Name

Phenyl-2-(S)-Aminopropane Saccharate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-1931

Substance

DEXTROAMPHETAMINE SACCHARATE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2012-10-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2015
30 Sep
Bulk Ingredient NDC: 59116-1932

Nonproprietary Name

Phenyl-2-(S)-Aminopropane Saccharate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-1932

Substance

DEXTROAMPHETAMINE SACCHARATE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2015-09-30

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
26 Oct
Bulk Ingredient NDC: 59116-1940

Nonproprietary Name

Phenyl-2-(S)-Aminopropane Sulfate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-1940

Substance

DEXTROAMPHETAMINE SULFATE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2012-10-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
26 Oct
Bulk Ingredient NDC: 59116-1941

Nonproprietary Name

Phenyl-2-(S)-Aminopropane Sulfate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-1941

Substance

DEXTROAMPHETAMINE SULFATE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2012-10-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
26 Oct
Bulk Ingredient NDC: 59116-1942

Nonproprietary Name

(S)-Alpha-Methylphenethylamine Sulphate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-1942

Substance

DEXTROAMPHETAMINE SULFATE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2012-10-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
26 Oct
Bulk Ingredient NDC: 59116-1960

Nonproprietary Name

Phenyl-2-(R,S)-Aminopropane Aspartate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-1960

Substance

AMPHETAMINE ASPARTATE MONOHYDRATE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2012-10-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
26 Oct
Bulk Ingredient NDC: 59116-1961

Nonproprietary Name

Phenyl-2-(R,S)-Aminopropane Aspartate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-1961

Substance

AMPHETAMINE ASPARTATE MONOHYDRATE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2012-10-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
26 Oct
Bulk Ingredient NDC: 59116-1962

Nonproprietary Name

Phenyl-2-(R,S)-Aminopropane Aspartate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-1962

Substance

AMPHETAMINE ASPARTATE MONOHYDRATE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2012-10-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2013
01 Nov
Bulk Ingredient NDC: 59116-1963

Nonproprietary Name

Phenyl-2-(R,S)-Aminopropane Aspartate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-1963

Substance

AMPHETAMINE ASPARTATE MONOHYDRATE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2013-11-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2015
30 Sep
Bulk Ingredient NDC: 59116-1964

Nonproprietary Name

Phenyl-2-(R,S)-Aminopropane Aspartate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-1964

Substance

AMPHETAMINE ASPARTATE MONOHYDRATE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2015-09-30

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
26 Oct
Bulk Ingredient NDC: 59116-1970

Nonproprietary Name

Phenyl-2-(R,S)-Aminopropane Sulfate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-1970

Substance

AMPHETAMINE SULFATE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2012-10-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
26 Oct
Bulk Ingredient NDC: 59116-1971

Nonproprietary Name

Phenyl-2-(R,S)-Aminopropane Sulfate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-1971

Substance

AMPHETAMINE SULFATE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2012-10-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
26 Oct
Bulk Ingredient NDC: 59116-2640

Nonproprietary Name

Fentanyl

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-2640

Substance

FENTANYL

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2012-10-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
26 Oct
Bulk Ingredient NDC: 59116-2641

Nonproprietary Name

Fentanyl

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-2641

Substance

FENTANYL

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2012-10-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
26 Oct
Bulk Ingredient NDC: 59116-2642

Nonproprietary Name

Fentanyl

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-2642

Substance

FENTANYL

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2012-10-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
26 Oct
Bulk Ingredient NDC: 59116-2643

Nonproprietary Name

Fentanyl

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-2643

Substance

FENTANYL

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2012-10-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
26 Oct
Bulk Ingredient NDC: 59116-2644

Nonproprietary Name

Fentanyl

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-2644

Substance

FENTANYL

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2012-10-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2018
01 Jan
Bulk Ingredient NDC: 59116-2645

Nonproprietary Name

Fentanyl

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-2645

Substance

FENTANYL

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2018-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2018
01 Jan
Bulk Ingredient NDC: 59116-2646

Nonproprietary Name

Fentanyl

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-2646

Substance

FENTANYL

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2018-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
26 Oct
Bulk Ingredient NDC: 59116-2900

Nonproprietary Name

Aripiprazole

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-2900

Substance

ARIPIPRAZOLE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-10-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
26 Oct
Bulk Ingredient NDC: 59116-2901

Nonproprietary Name

Aripiprazole

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-2901

Substance

ARIPIPRAZOLE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-10-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
26 Oct
Bulk Ingredient NDC: 59116-3010

Nonproprietary Name

Lisdexamfetamine Dimesylate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-3010

Substance

LISDEXAMFETAMINE DIMESYLATE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2012-10-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2013
02 Jul
Bulk Ingredient NDC: 59116-3011

Nonproprietary Name

Lisdexamfetamine Dimesylate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-3011

Substance

LISDEXAMFETAMINE DIMESYLATE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2013-07-02

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2014
01 Jan
Bulk Ingredient NDC: 59116-3012

Nonproprietary Name

Lisdexamfetamine Dimesylate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-3012

Substance

LISDEXAMFETAMINE DIMESYLATE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2014-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2016
14 Oct
Bulk Ingredient NDC: 59116-3013

Nonproprietary Name

Lisdexamfetamine Dimesylate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-3013

Substance

LISDEXAMFETAMINE DIMESYLATE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2016-10-14

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2012
26 Oct
Bulk Ingredient NDC: 59116-3280

Nonproprietary Name

Fentanyl Citrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-3280

Substance

FENTANYL CITRATE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2012-10-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
26 Oct
Bulk Ingredient NDC: 59116-3281

Nonproprietary Name

Fentanyl Citrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-3281

Substance

FENTANYL CITRATE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2012-10-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
26 Oct
Bulk Ingredient NDC: 59116-3282

Nonproprietary Name

Fentanyl Citrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-3282

Substance

FENTANYL CITRATE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2012-10-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
26 Oct
Bulk Ingredient NDC: 59116-3390

Nonproprietary Name

Methylphenidate Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-3390

Substance

METHYLPHENIDATE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2012-10-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
26 Oct
Bulk Ingredient NDC: 59116-3391

Nonproprietary Name

Methylphenidate Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-3391

Substance

METHYLPHENIDATE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2012-10-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2013
01 Sep
Bulk Ingredient NDC: 59116-3392

Nonproprietary Name

Methylphenidate Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-3392

Substance

METHYLPHENIDATE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2013-09-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2013
01 Aug
Bulk Ingredient NDC: 59116-3393

Nonproprietary Name

Methylphenidate Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-3393

Substance

METHYLPHENIDATE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2013-08-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2015
01 Jun
Bulk Ingredient NDC: 59116-3394

Nonproprietary Name

Methylphenidate Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-3394

Substance

METHYLPHENIDATE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2015-06-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
26 Oct
Bulk Ingredient NDC: 59116-3610

Nonproprietary Name

Nicotine Resinate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-3610

Substance

NICOTINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-10-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
26 Oct
Bulk Ingredient NDC: 59116-3611

Nonproprietary Name

Nicotine Resinate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-3611

Substance

NICOTINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-10-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
26 Oct
Bulk Ingredient NDC: 59116-3612

Nonproprietary Name

Nicotine Resinate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-3612

Substance

NICOTINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-10-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
26 Oct
Bulk Ingredient NDC: 59116-3613

Nonproprietary Name

Nicotine Resinate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-3613

Substance

NICOTINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-10-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
26 Oct
Bulk Ingredient NDC: 59116-3614

Nonproprietary Name

Nicotine Resinate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-3614

Substance

NICOTINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-10-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
26 Oct
Bulk Ingredient NDC: 59116-3615

Nonproprietary Name

Nicotine Polacrilex

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-3615

Substance

NICOTINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-10-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2015
28 Sep
Bulk Ingredient NDC: 59116-4030

Nonproprietary Name

Rose Bengal Lactone

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-4030

Substance

ROSE BENGAL LACTONE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2015-09-28

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2014
25 Mar
Bulk Ingredient NDC: 59116-4250

Nonproprietary Name

Erlotinib HCl

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-4250

Substance

ERLOTINIB HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-03-25

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2014
01 Jun
Bulk Ingredient NDC: 59116-4251

Nonproprietary Name

Erlotinib HCl

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-4251

Substance

ERLOTINIB HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-06-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2013
29 Mar
Bulk Ingredient NDC: 59116-4290

Nonproprietary Name

Naloxegol Oxalate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-4290

Substance

NALOXEGOL OXALATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2013-03-29

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2014
08 Aug
Bulk Ingredient NDC: 59116-4480

Nonproprietary Name

Lapatinib Ditosylate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-4480

Substance

LAPATINIB DITOSYLATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-08-08

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
26 Oct
Bulk Ingredient NDC: 59116-4490

Nonproprietary Name

Camouflage Hydrocodone

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-4490

Substance

HYDROCODONE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2012-10-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
26 Oct
Bulk Ingredient NDC: 59116-4580

Nonproprietary Name

Opium Tincture

Dosage Form

LIQUID

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-4580

Substance

OPIUM

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2012-10-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2013
25 Nov
Bulk Ingredient NDC: 59116-4670

Nonproprietary Name

Sofosbuvir

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-4670

Substance

SOFOSBUVIR

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2013-11-25

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2014
30 Jun
Bulk Ingredient NDC: 59116-4710

Nonproprietary Name

Lenalidomide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-4710

Substance

LENALIDOMIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-06-30

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
26 Oct
Bulk Ingredient NDC: 59116-4730

Nonproprietary Name

Camouflage Chlorpheniramine

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-4730

Substance

CHLORPHENIRAMINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-10-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2014
01 Oct
Bulk Ingredient NDC: 59116-4750

Nonproprietary Name

Hydrocodone Bitartrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-4750

Substance

HYDROCODONE BITARTRATE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2014-10-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2014
01 Oct
Bulk Ingredient NDC: 59116-4751

Nonproprietary Name

Hydrocodone Bitartrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-4751

Substance

HYDROCODONE BITARTRATE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2014-10-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2015
31 Jul
Bulk Ingredient NDC: 59116-4760

Nonproprietary Name

Hydromorphone Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-4760

Substance

HYDROMORPHONE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2015-07-31

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2016
01 Dec
Bulk Ingredient NDC: 59116-4950

Nonproprietary Name

Capromorelin Tartrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-4950

Substance

CAPROMORELIN TARTRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2016-12-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2015
20 Aug
Bulk Ingredient NDC: 59116-4970

Nonproprietary Name

Soluble Ferric Pyrophosphate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-4970

Substance

FERRIC PYROPHOSPHATE CITRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2015-08-20

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2017
01 Jan
Bulk Ingredient NDC: 59116-4971

Nonproprietary Name

Soluble Ferric Pyrophosphate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-4971

Substance

FERRIC PYROPHOSPHATE CITRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2017-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2018
31 Jul
Bulk Ingredient NDC: 59116-4980

Nonproprietary Name

Buprenorphine HCl

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-4980

Substance

BUPRENORPHINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

CIII

Start Marketing Date

2018-07-31

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2015
21 Aug
Bulk Ingredient NDC: 59116-4990

Nonproprietary Name

Phenyl-2-(R,S)-Aminopropane L-Aspartate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-4990

Substance

AMPHETAMINE ASPARTATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2015-08-21

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2017
19 Sep
Bulk Ingredient NDC: 59116-5070

Nonproprietary Name

Aripiprazole Lauroxil

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-5070

Substance

ARIPIPRAZOLE LAUROXIL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2017-09-19

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2018
01 Aug
Bulk Ingredient NDC: 59116-5161

Nonproprietary Name

Samidorphan L-Malate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-5161

Substance

SAMIDORPHAN L-MALATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2018-08-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2018
01 Aug
Bulk Ingredient NDC: 59116-5162

Nonproprietary Name

Samidorphan L-Malate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-5162

Substance

SAMIDORPHAN L-MALATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2018-08-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2018
01 Aug
Bulk Ingredient NDC: 59116-5163

Nonproprietary Name

Samidorphan L-Malate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-5163

Substance

SAMIDORPHAN L-MALATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2018-08-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2018
01 Aug
Bulk Ingredient NDC: 59116-5164

Nonproprietary Name

Samidorphan L-Malate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-5164

Substance

SAMIDORPHAN L-MALATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2018-08-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2018
01 Aug
Bulk Ingredient NDC: 59116-5165

Nonproprietary Name

Samidorphan L-Malate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-5165

Substance

SAMIDORPHAN L-MALATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2018-08-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2017
15 Aug
Bulk Ingredient NDC: 59116-5170

Nonproprietary Name

Lifitegrast

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-5170

Substance

LIFITEGRAST

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2017-08-15

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
24 Feb
Bulk Ingredient NDC: 59116-5330

Nonproprietary Name

Ripretinib

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-5330

Substance

RIPRETINIB

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-02-24

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
24 Feb
Bulk Ingredient NDC: 59116-5331

Nonproprietary Name

Ripretinib

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-5331

Substance

RIPRETINIB

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-02-24

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
24 Feb
Bulk Ingredient NDC: 59116-5332

Nonproprietary Name

Ripretinib

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-5332

Substance

RIPRETINIB

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-02-24

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
24 Feb
Bulk Ingredient NDC: 59116-5333

Nonproprietary Name

Ripretinib

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-5333

Substance

RIPRETINIB

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-02-24

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
01 Apr
Bulk Ingredient NDC: 59116-5440

Nonproprietary Name

FIlgotinib Maleate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-5440

Substance

FILGOTINIB MALEATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-04-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
04 Feb
Bulk Ingredient NDC: 59116-5720

Nonproprietary Name

Voxelotor

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-5720

Substance

VOXELOTOR

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-02-04

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
30 Dec
Bulk Ingredient NDC: 59116-5910

Nonproprietary Name

Acoramidis HCl

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-5910

Substance

ACORAMIDIS HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-12-30

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
30 Dec
Bulk Ingredient NDC: 59116-5911

Nonproprietary Name

Acoramidis HCl Milled

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-5911

Substance

ACORAMIDIS HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-12-30

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
14 Dec
Bulk Ingredient NDC: 59116-5950

Nonproprietary Name

Sodium Oxybate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-5950

Substance

SODIUM OXYBATE

Product Type

BULK INGREDIENT

DEA Schedule

CI

Start Marketing Date

2021-12-14

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
14 Dec
Bulk Ingredient NDC: 59116-5960

Nonproprietary Name

Potassium Oxybate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-5960

Substance

POTASSIUM OXYBATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-12-14

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
14 Dec
Bulk Ingredient NDC: 59116-5980

Nonproprietary Name

Magnesium Oxybate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-5980

Substance

MAGNESIUM OXYBATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-12-14

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
04 Feb
Bulk Ingredient NDC: 59116-6030

Nonproprietary Name

Sodium Thiosulfate Anhydrous

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-6030

Substance

SODIUM THIOSULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-02-04

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
15 Oct
Bulk Ingredient NDC: 59116-6490

Nonproprietary Name

Remdesivir

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-6490

Substance

REMDESIVIR

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-10-15

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
28 Jun
Bulk Ingredient NDC: 59116-6850

Nonproprietary Name

Methylphenidate Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-6850

Substance

METHYLPHENIDATE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2022-06-28

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
16 Dec
Bulk Ingredient NDC: 59116-7110

Nonproprietary Name

Filgotinib Maleate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-7110

Substance

FILGOTINIB MALEATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-12-16

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2013
01 Aug
Bulk Ingredient NDC: 59116-7560

Nonproprietary Name

Methylphenidate Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc

Marketing Category

BULK INGREDIENT

59116-7560

Substance

METHYLPHENIDATE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2013-08-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
18 Nov
Bulk Ingredient NDC: 59116-0691

Nonproprietary Name

TAK-279

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc.

Marketing Category

BULK INGREDIENT

59116-0691

Substance

ZASOCITINIB

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2022-11-18

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2013
29 Mar
Bulk Ingredient NDC: 59116-4290

Nonproprietary Name

Naloxegol Oxalate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc.

Marketing Category

BULK INGREDIENT

59116-4290

Substance

NALOXEGOL OXALATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2013-03-29

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2018
28 Jun
Bulk Ingredient NDC: 59116-5570

Nonproprietary Name

Berotralstat hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc.

Marketing Category

BULK INGREDIENT

59116-5570

Substance

BEROTRALSTAT HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2018-06-28

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
31 Mar
Bulk Ingredient NDC: 59116-5970

Nonproprietary Name

Calcium Oxybate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc.

Marketing Category

BULK INGREDIENT

59116-5970

Substance

CALCIUM OXYBATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2022-03-31

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
28 Feb
Bulk Ingredient NDC: 59116-6031

Nonproprietary Name

Sodium Thiosulfate Anhydrous

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc.

Marketing Category

BULK INGREDIENT

59116-6031

Substance

SODIUM THIOSULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-02-28

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
06 Apr
Bulk Ingredient NDC: 59116-6280

Nonproprietary Name

CK-3773274

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc.

Marketing Category

BULK INGREDIENT

59116-6280

Substance

AFICAMTEN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-04-06

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
12 Feb
Bulk Ingredient NDC: 59116-6360

Nonproprietary Name

trilaciclib dihydrochloride dihydrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc.

Marketing Category

BULK INGREDIENT

59116-6360

Substance

TRILACICLIB DIHYDROCHLORIDE DIHYDRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-02-12

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
15 Oct
Bulk Ingredient NDC: 59116-6490

Nonproprietary Name

Remdesivir

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc.

Marketing Category

BULK INGREDIENT

59116-6490

Substance

REMDESIVIR

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-10-15

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
04 Jan
Bulk Ingredient NDC: 59116-6640

Nonproprietary Name

Flibanserin

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc.

Marketing Category

BULK INGREDIENT

59116-6640

Substance

FLIBANSERIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2022-01-04

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
01 Feb
Bulk Ingredient NDC: 59116-6870

Nonproprietary Name

UTENPANIUM CHLORIDE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc.

Marketing Category

BULK INGREDIENT

59116-6870

Substance

UTENPANIUM CHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2022-02-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
18 Nov
Bulk Ingredient NDC: 59116-6910

Nonproprietary Name

NDI-034858

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc.

Marketing Category

BULK INGREDIENT

59116-6910

Substance

ZASOCITINIB

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2022-11-18

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2020
04 Mar
Bulk Ingredient NDC: 59116-6970

Nonproprietary Name

ALXN2040

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc.

Marketing Category

BULK INGREDIENT

59116-6970

Substance

DANICOPAN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-03-04

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
18 Nov
Bulk Ingredient NDC: 59116-7030

Nonproprietary Name

TAK-018

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc.

Marketing Category

BULK INGREDIENT

59116-7030

Substance

SIBOFIMLOC

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2022-11-18

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
22 May
Bulk Ingredient NDC: 59116-7160

Nonproprietary Name

CLN-081

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc.

Marketing Category

BULK INGREDIENT

59116-7160

Substance

ZIPALERTINIB

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-05-22

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
20 Mar
Bulk Ingredient NDC: 59116-7270

Nonproprietary Name

S225SS Milled

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc.

Marketing Category

BULK INGREDIENT

59116-7270

Substance

ENSITRELVIR FUMARATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-03-20

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
13 Jun
Bulk Ingredient NDC: 59116-7280

Nonproprietary Name

AZD9833

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc.

Marketing Category

BULK INGREDIENT

59116-7280

Substance

CAMIZESTRANT

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-06-13

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
23 Oct
Bulk Ingredient NDC: 59116-7320

Nonproprietary Name

RPT193-1 Hemi-Tartrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc.

Marketing Category

BULK INGREDIENT

59116-7320

Substance

ZELNECIRNON

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-10-23

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
25 Jul
Bulk Ingredient NDC: 59116-7330

Nonproprietary Name

Ferric Maltol

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc.

Marketing Category

BULK INGREDIENT

59116-7330

Substance

FERRIC MALTOL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-07-25

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2014
24 Sep
Bulk Ingredient NDC: 59116-7480

Nonproprietary Name

GS-9036

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc.

Marketing Category

BULK INGREDIENT

59116-7480

Substance

EMTRICITABINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-09-24

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
02 Mar
Bulk Ingredient NDC: 59116-7530

Nonproprietary Name

SDX

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Charles City, Inc.

Marketing Category

BULK INGREDIENT

59116-7530

Substance

SERDEXMETHYLPHENIDATE CHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-03-02

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2016
19 Jul
Bulk Ingredient NDC: 12651-111

Nonproprietary Name

BUPIVACAINE HYDROCHLORIDE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Karlskoga AB

Marketing Category

BULK INGREDIENT

12651-111

Substance

BUPIVACAINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2016-07-19

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2006
30 Jun
Bulk Ingredient NDC: 12651-113

Nonproprietary Name

Lidocaine hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Karlskoga AB

Marketing Category

BULK INGREDIENT

12651-113

Substance

LIDOCAINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2006-06-30

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2000
27 Dec
Bulk Ingredient NDC: 12651-115

Nonproprietary Name

Benzoyl peroxide, hydrous

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Karlskoga AB

Marketing Category

BULK INGREDIENT

12651-115

Substance

BENZOYL PEROXIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2000-12-27

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2011
01 Aug
Bulk Ingredient NDC: 12651-116

Nonproprietary Name

Bupivacaine base

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Karlskoga AB

Marketing Category

BULK INGREDIENT

12651-116

Substance

BUPIVACAINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2011-08-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2017
22 Feb
Bulk Ingredient NDC: 12651-118

Nonproprietary Name

RIVASTIGMINE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Karlskoga AB

Marketing Category

BULK INGREDIENT

12651-118

Substance

RIVASTIGMINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2017-02-22

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
05 Mar
Bulk Ingredient NDC: 12651-119

Nonproprietary Name

4-Amiinobenzoic acid

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Karlskoga AB

Marketing Category

BULK INGREDIENT

12651-119

Substance

AMINOBENZOIC ACID

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-03-05

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
13 Jan
Bulk Ingredient NDC: 12651-120

Nonproprietary Name

Berotralstat Dihydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Karlskoga AB

Marketing Category

BULK INGREDIENT

12651-120

Substance

BEROTRALSTAT DIHYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-01-13

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
19 Jan
Bulk Ingredient NDC: 12651-121

Nonproprietary Name

Tesofensine/NS2330 citrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Karlskoga AB

Marketing Category

BULK INGREDIENT

12651-121

Substance

TESOFENSINE CITRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-01-19

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
08 Feb
Bulk Ingredient NDC: 12651-123

Nonproprietary Name

Momelotinib dihydrochloride monohydrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Karlskoga AB

Marketing Category

BULK INGREDIENT

12651-123

Substance

MOMELOTINIB DIHYDROCHLORIDE MONOHYDRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-02-08

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
12 Oct
Bulk Ingredient NDC: 12651-124

Nonproprietary Name

LIDOCAINE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Karlskoga AB

Marketing Category

BULK INGREDIENT

12651-124

Substance

LIDOCAINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-10-12

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
31 Oct
Bulk Ingredient NDC: 12651-125

Nonproprietary Name

Olanzapine

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Karlskoga AB

Marketing Category

BULK INGREDIENT

12651-125

Substance

OLANZAPINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-10-31

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1988
21 Mar
Bulk Ingredient NDC: 12651-582

Nonproprietary Name

Mesalamine

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Karlskoga AB

Marketing Category

BULK INGREDIENT

12651-582

Substance

MESALAMINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1988-03-21

End Marketing Date

-

Listing Record Certified Through

2027-12-31

1986
28 Apr
Bulk Ingredient NDC: 12828-0004

Nonproprietary Name

Chlordiazepoxide Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Profarmaco Milano Srl

Marketing Category

BULK INGREDIENT

12828-0004

Substance

CHLORDIAZEPOXIDE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

CIV

Start Marketing Date

1986-04-28

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1986
27 Jan
Bulk Ingredient NDC: 12828-0005

Nonproprietary Name

Chlorothiazide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Profarmaco Milano Srl

Marketing Category

BULK INGREDIENT

12828-0005

Substance

CHLOROTHIAZIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1986-01-27

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1986
12 Sep
Bulk Ingredient NDC: 12828-0006

Nonproprietary Name

Chlordiazepoxide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Profarmaco Milano Srl

Marketing Category

BULK INGREDIENT

12828-0006

Substance

CHLORDIAZEPOXIDE

Product Type

BULK INGREDIENT

DEA Schedule

CIV

Start Marketing Date

1986-09-12

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1986
21 Jan
Bulk Ingredient NDC: 12828-0008

Nonproprietary Name

Hydrochlorothiazide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Profarmaco Milano Srl

Marketing Category

BULK INGREDIENT

12828-0008

Substance

HYDROCHLOROTHIAZIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1986-01-21

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1986
18 Apr
Bulk Ingredient NDC: 12828-0013

Nonproprietary Name

Diazepam

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Profarmaco Milano Srl

Marketing Category

BULK INGREDIENT

12828-0013

Substance

DIAZEPAM

Product Type

BULK INGREDIENT

DEA Schedule

CIV

Start Marketing Date

1986-04-18

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1986
24 Jan
Bulk Ingredient NDC: 12828-0015

Nonproprietary Name

Bisacodyl

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Profarmaco Milano Srl

Marketing Category

BULK INGREDIENT

12828-0015

Substance

BISACODYL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1986-01-24

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1986
18 Apr
Bulk Ingredient NDC: 12828-0017

Nonproprietary Name

Flurazepam Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Profarmaco Milano Srl

Marketing Category

BULK INGREDIENT

12828-0017

Substance

FLURAZEPAM HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

CIV

Start Marketing Date

1986-04-18

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1996
16 Oct
Bulk Ingredient NDC: 12828-0018

Nonproprietary Name

Amiodarone HCl

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Profarmaco Milano Srl

Marketing Category

BULK INGREDIENT

12828-0018

Substance

AMIODARONE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1996-10-16

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1987
26 Mar
Bulk Ingredient NDC: 12828-0019

Nonproprietary Name

Clorazepate Dipotassium

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Profarmaco Milano Srl

Marketing Category

BULK INGREDIENT

12828-0019

Substance

CLORAZEPATE DIPOTASSIUM

Product Type

BULK INGREDIENT

DEA Schedule

CIV

Start Marketing Date

1987-03-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2016
09 Dec
Bulk Ingredient NDC: 12828-0021

Nonproprietary Name

LORMETAZEPAM

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

CAMBREX PROFARMACO MILANO SRL

Marketing Category

BULK INGREDIENT

12828-0021

Substance

LORMETAZEPAM

Product Type

BULK INGREDIENT

DEA Schedule

CIV

Start Marketing Date

2016-12-09

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1986
01 May
Bulk Ingredient NDC: 12828-0022

Nonproprietary Name

Temazepam

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Profarmaco Milano Srl

Marketing Category

BULK INGREDIENT

12828-0022

Substance

TEMAZEPAM

Product Type

BULK INGREDIENT

DEA Schedule

CIV

Start Marketing Date

1986-05-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1986
30 Apr
Bulk Ingredient NDC: 12828-0023

Nonproprietary Name

Methyclothiazide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Profarmaco Milano Srl

Marketing Category

BULK INGREDIENT

12828-0023

Substance

METHYCLOTHIAZIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1986-04-30

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1986
21 May
Bulk Ingredient NDC: 12828-0024

Nonproprietary Name

Oxazepam

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Profarmaco Milano Srl

Marketing Category

BULK INGREDIENT

12828-0024

Substance

OXAZEPAM

Product Type

BULK INGREDIENT

DEA Schedule

CIV

Start Marketing Date

1986-05-21

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1987
12 Mar
Bulk Ingredient NDC: 12828-0025

Nonproprietary Name

Lorazepam

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Profarmaco Milano Srl

Marketing Category

BULK INGREDIENT

12828-0025

Substance

LORAZEPAM

Product Type

BULK INGREDIENT

DEA Schedule

CIV

Start Marketing Date

1987-03-12

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1995
11 Apr
Bulk Ingredient NDC: 12828-0034

Nonproprietary Name

Amiloride HCl

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Profarmaco Milano Srl

Marketing Category

BULK INGREDIENT

12828-0034

Substance

AMILORIDE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1995-04-11

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1986
24 Jun
Bulk Ingredient NDC: 12828-0037

Nonproprietary Name

Diltiazem Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Profarmaco Milano Srl

Marketing Category

BULK INGREDIENT

12828-0037

Substance

DILTIAZEM HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1986-06-24

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1988
04 Apr
Bulk Ingredient NDC: 12828-0040

Nonproprietary Name

Alprazolam

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Profarmaco Milano Srl

Marketing Category

BULK INGREDIENT

12828-0040

Substance

ALPRAZOLAM

Product Type

BULK INGREDIENT

DEA Schedule

CIV

Start Marketing Date

1988-04-04

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1986
12 Aug
Bulk Ingredient NDC: 12828-0041

Nonproprietary Name

Triazolam

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Profarmaco Milano Srl

Marketing Category

BULK INGREDIENT

12828-0041

Substance

TRIAZOLAM

Product Type

BULK INGREDIENT

DEA Schedule

CIV

Start Marketing Date

1986-08-12

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1993
05 Jan
Bulk Ingredient NDC: 12828-0051

Nonproprietary Name

Glipizide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Profarmaco Milano Srl

Marketing Category

BULK INGREDIENT

12828-0051

Substance

GLIPIZIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1993-01-05

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1998
21 Aug
Bulk Ingredient NDC: 12828-0053

Nonproprietary Name

Terbutaline Sulfate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Profarmaco Milano Srl

Marketing Category

BULK INGREDIENT

12828-0053

Substance

TERBUTALINE SULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1998-08-21

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1996
08 Mar
Bulk Ingredient NDC: 12828-0060

Nonproprietary Name

Clonazepam

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Profarmaco Milano Srl

Marketing Category

BULK INGREDIENT

12828-0060

Substance

CLONAZEPAM

Product Type

BULK INGREDIENT

DEA Schedule

CIV

Start Marketing Date

1996-03-08

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1993
17 Feb
Bulk Ingredient NDC: 12828-0062

Nonproprietary Name

Cromolyn Sodium

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Profarmaco Milano Srl

Marketing Category

BULK INGREDIENT

12828-0062

Substance

CROMOLYN SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1993-02-17

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1986
21 May
Bulk Ingredient NDC: 12828-0063

Nonproprietary Name

Albuterol Sulfate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Profarmaco Milano Srl

Marketing Category

BULK INGREDIENT

12828-0063

Substance

ALBUTEROL SULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1986-05-21

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2000
07 Sep
Bulk Ingredient NDC: 12828-0064

Nonproprietary Name

Norepinephrine Bitartrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Profarmaco Milano Srl

Marketing Category

BULK INGREDIENT

12828-0064

Substance

NOREPINEPHRINE BITARTRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2000-09-07

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1993
01 Feb
Bulk Ingredient NDC: 12828-0066

Nonproprietary Name

Glyburide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Profarmaco Milano Srl

Marketing Category

BULK INGREDIENT

12828-0066

Substance

GLYBURIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1993-02-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1993
22 Feb
Bulk Ingredient NDC: 12828-0068

Nonproprietary Name

Cysteamine Bitartrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Profarmaco Milano Srl

Marketing Category

BULK INGREDIENT

12828-0068

Substance

CYSTEAMINE BITARTRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1993-02-22

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1996
03 Oct
Bulk Ingredient NDC: 12828-0069

Nonproprietary Name

Midazolam

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Profarmaco Milano Srl

Marketing Category

BULK INGREDIENT

12828-0069

Substance

MIDAZOLAM

Product Type

BULK INGREDIENT

DEA Schedule

CIV

Start Marketing Date

1996-10-03

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1996
11 Nov
Bulk Ingredient NDC: 12828-0070

Nonproprietary Name

Labetalol Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Profarmaco Milano Srl

Marketing Category

BULK INGREDIENT

12828-0070

Substance

LABETALOL HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1996-11-11

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1996
05 Dec
Bulk Ingredient NDC: 12828-0071

Nonproprietary Name

Sotalol Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Profarmaco Milano Srl

Marketing Category

BULK INGREDIENT

12828-0071

Substance

SOTALOL HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1996-12-05

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1996
05 Dec
Bulk Ingredient NDC: 12828-0072

Nonproprietary Name

Clozapine

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Profarmaco Milano Srl

Marketing Category

BULK INGREDIENT

12828-0072

Substance

CLOZAPINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1996-12-05

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2002
28 Jan
Bulk Ingredient NDC: 12828-0077

Nonproprietary Name

Estazolam

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Profarmaco Milano Srl

Marketing Category

BULK INGREDIENT

12828-0077

Substance

ESTAZOLAM

Product Type

BULK INGREDIENT

DEA Schedule

CIV

Start Marketing Date

2002-01-28

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2011
19 Jan
Bulk Ingredient NDC: 12828-0081

Nonproprietary Name

Sodium Picosulfate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Profarmaco Milano Srl

Marketing Category

BULK INGREDIENT

12828-0081

Substance

SODIUM PICOSULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2011-01-19

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
01 Aug
Bulk Ingredient NDC: 12828-0082

Nonproprietary Name

Epinephrine

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Profarmaco Milano Srl

Marketing Category

BULK INGREDIENT

12828-0082

Substance

EPINEPHRINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-08-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2014
03 Jun
Bulk Ingredient NDC: 12828-0083

Nonproprietary Name

Epinephrine Bitartrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Profarmaco Milano Srl

Marketing Category

BULK INGREDIENT

12828-0083

Substance

EPINEPHRINE BITARTRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-06-03

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2016
21 Jul
Bulk Ingredient NDC: 12828-0084

Nonproprietary Name

Clobazam

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

CAMBREX PROFARMACO MILANO SRL

Marketing Category

BULK INGREDIENT

12828-0084

Substance

CLOBAZAM

Product Type

BULK INGREDIENT

DEA Schedule

CIV

Start Marketing Date

2016-07-21

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2011
03 Jan
Bulk Ingredient NDC: 12828-0085

Nonproprietary Name

Raloxifene Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Profarmaco Milano Srl

Marketing Category

BULK INGREDIENT

12828-0085

Substance

RALOXIFENE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2011-01-03

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
18 Jun
Bulk Ingredient NDC: 12828-0086

Nonproprietary Name

Zolpidem Tartrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Profarmaco Milano Srl

Marketing Category

BULK INGREDIENT

12828-0086

Substance

ZOLPIDEM TARTRATE

Product Type

BULK INGREDIENT

DEA Schedule

CIV

Start Marketing Date

2012-06-18

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2016
21 Jul
Bulk Ingredient NDC: 12828-0087

Nonproprietary Name

LACOSAMIDE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

CAMBREX PROFARMACO MILANO SRL

Marketing Category

BULK INGREDIENT

12828-0087

Substance

LACOSAMIDE

Product Type

BULK INGREDIENT

DEA Schedule

CV

Start Marketing Date

2016-07-21

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2014
01 Dec
Bulk Ingredient NDC: 12828-0088

Nonproprietary Name

Aripiprazole

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cambrex Profarmaco Milano Srl

Marketing Category

BULK INGREDIENT

12828-0088

Substance

ARIPIPRAZOLE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-12-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
24 Sep
Bulk Ingredient NDC: 12828-0091

Nonproprietary Name

MARAVIROC

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

CAMBREX PROFARMACO MILANO SRL

Marketing Category

BULK INGREDIENT

12828-0091

Substance

MARAVIROC

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-09-24

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
18 Oct
Bulk Ingredient NDC: 12828-0092

Nonproprietary Name

MIDAZOLAM HCL

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

CAMBREX PROFARMACO MILANO SRL

Marketing Category

BULK INGREDIENT

12828-0092

Substance

MIDAZOLAM HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

CIV

Start Marketing Date

2021-10-18

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
04 Aug
Bulk Ingredient NDC: 12828-0093

Nonproprietary Name

AMBROXOL HCL

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

CAMBREX PROFARMACO MILANO SRL

Marketing Category

BULK INGREDIENT

12828-0093

Substance

AMBROXOL HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2022-08-04

End Marketing Date

-

Listing Record Certified Through

2026-12-31

Related Databases
  • FDA Inspections
    26 View
  • EDQM CEP
    36 View
  • KDMF
    0 View
  • Japan DMF
    9 View
  • Eudra GMP
    0 View
  • NDC Database
    168 View
  • FDA Approved Drugs Database
    0 View
NDC Type Breakdown
168 total
  • Bulk Ingredient
Official Source

NDC data is based on publicly available National Drug Code information from the U.S. Food and Drug Administration (FDA).

Visit FDA NDC Directory
NDC Record Details Preview

Explore important National Drug Code information available in the records above.

NDC

59116-0630

Nonproprietary Name

Sulfasalazine

Labeler

Cambrex Charles City, Inc

Dosage Form

POWDER

FDA NDC Data

National Drug Code information

Regular Updates

Data maintained from official sources

Structured Database

Searchable pharmaceutical data

Reliable Data

Organized NDC records

NDC data is based on publicly available U.S. Food and Drug Administration (FDA) National Drug Code information.

Create a New Buying Request

Fields marked with * are mandatory.

Please enter quantity.
Please select a unit.
Please select quality standard.
Please select request type.
Please provide product specifications.
Please enter additional details.
Please select shipping preference.
Notice: By submitting this buying request, the provided product details and requirements may be published publicly on our marketplace.