Siegfried AG
NDC Database

Siegfried AG

NDC Database

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

Bulk Ingredient Drug for Further Processing
  • Total Records 54
  • Latest Marketing Date 2024-11-06
  • Data Source FDA
  • First Marketing Date 1967-03-21
All
54
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Bulk Ingredient
52
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Drug for Further Processing
2
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Company Overview

Company

Siegfried AG

Country

Switzerland

Social Profiles

LinkedIn X / Twitter
Company Snapshot

Siegfried AG

Untere Bruehlstrasse 4, 4800 Zofingen

Switzerland

www.siegfried.ch/ info@siegfried.ch View on Map
NDC Records ( 54 records )
1996
24 Dec
Bulk Ingredient NDC: 17205-096

Nonproprietary Name

Topiramate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried AG

Marketing Category

BULK INGREDIENT

17205-096

Substance

TOPIRAMATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1996-12-24

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
12 Apr
Bulk Ingredient NDC: 17205-097

Nonproprietary Name

Oclacitinib Maleate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried AG

Marketing Category

BULK INGREDIENT

17205-097

Substance

OCLACITINIB MALEATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-04-12

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2016
29 Apr
Bulk Ingredient NDC: 17205-098

Nonproprietary Name

Pimavanserin Tartrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried AG

Marketing Category

BULK INGREDIENT

17205-098

Substance

PIMAVANSERIN TARTRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2016-04-29

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
31 Jan
Bulk Ingredient NDC: 17205-099

Nonproprietary Name

Sarolaner

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried AG

Marketing Category

BULK INGREDIENT

17205-099

Substance

SAROLANER

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-01-31

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2010
27 Jan
Bulk Ingredient NDC: 17205-100

Nonproprietary Name

Buprenorphine Base

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried AG

Marketing Category

BULK INGREDIENT

17205-100

Substance

BUPRENORPHINE

Product Type

BULK INGREDIENT

DEA Schedule

CIII

Start Marketing Date

2010-01-27

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2010
01 Mar
Bulk Ingredient NDC: 17205-101

Nonproprietary Name

Naloxone Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried AG

Marketing Category

BULK INGREDIENT

17205-101

Substance

NALOXONE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2010-03-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2010
14 Apr
Bulk Ingredient NDC: 17205-102

Nonproprietary Name

Naltrexone Base

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried AG

Marketing Category

BULK INGREDIENT

17205-102

Substance

NALTREXONE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2010-04-14

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2010
01 Jan
Bulk Ingredient NDC: 17205-103

Nonproprietary Name

Naltrexone Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried AG

Marketing Category

BULK INGREDIENT

17205-103

Substance

NALTREXONE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2010-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1984
22 Oct
Bulk Ingredient NDC: 17205-104

Nonproprietary Name

Oxiconazole Nitrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried AG

Marketing Category

BULK INGREDIENT

17205-104

Substance

OXICONAZOLE NITRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1984-10-22

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2004
09 Mar
Bulk Ingredient NDC: 17205-105

Nonproprietary Name

Nicotine Bitartrate Dihydrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried AG

Marketing Category

BULK INGREDIENT

17205-105

Substance

NICOTINE BITARTRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2004-03-09

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2010
20 Apr
Bulk Ingredient NDC: 17205-107

Nonproprietary Name

Lacosamide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

SIEGFRIED AG

Marketing Category

BULK INGREDIENT

17205-107

Substance

LACOSAMIDE

Product Type

BULK INGREDIENT

DEA Schedule

CV

Start Marketing Date

2010-04-20

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2010
01 Jan
Bulk Ingredient NDC: 17205-108

Nonproprietary Name

Naltrexone Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried AG

Marketing Category

BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING

17205-108

Substance

NALTREXONE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2010-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
01 Apr
Drug for Further Processing NDC: 17205-205

Nonproprietary Name

THALIDOMIDE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried AG

Marketing Category

DRUG FOR FURTHER PROCESSING

17205-205

Substance

THALIDOMIDE

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

2023-04-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1973
07 Dec
Bulk Ingredient NDC: 17205-307

Nonproprietary Name

Primidone

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried AG

Marketing Category

BULK INGREDIENT

17205-307

Substance

PRIMIDONE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1973-12-07

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
30 Jun
Bulk Ingredient NDC: 17205-308

Nonproprietary Name

Primidone

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried AG

Marketing Category

BULK INGREDIENT

17205-308

Substance

PRIMIDONE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-06-30

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1996
21 Jun
Bulk Ingredient NDC: 17205-340

Nonproprietary Name

Proparacaine Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried AG

Marketing Category

BULK INGREDIENT

17205-340

Substance

PROPARACAINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1996-06-21

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1981
27 Feb
Bulk Ingredient NDC: 17205-416

Nonproprietary Name

Trimethobenzamide HCl

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried AG

Marketing Category

BULK INGREDIENT

17205-416

Substance

TRIMETHOBENZAMIDE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1981-02-27

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2007
12 Nov
Bulk Ingredient NDC: 17205-482

Nonproprietary Name

Buprenorphine HCl

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried AG

Marketing Category

BULK INGREDIENT

17205-482

Substance

BUPRENORPHINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

CIII

Start Marketing Date

2007-11-12

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
12 Dec
Bulk Ingredient NDC: 17205-483

Nonproprietary Name

Nicotine Polacrilex

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried AG

Marketing Category

BULK INGREDIENT

17205-483

Substance

NICOTINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-12-12

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2024
18 Apr
Bulk Ingredient NDC: 17205-567

Nonproprietary Name

Venlafaxine HCl

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried AG

Marketing Category

BULK INGREDIENT

17205-567

Substance

VENLAFAXINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-04-18

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1988
18 Nov
Bulk Ingredient NDC: 17205-601

Nonproprietary Name

Nicotine

Dosage Form

LIQUID

Strength

1 kg/kg

Labeler

Siegfried AG

Marketing Category

BULK INGREDIENT

17205-601

Substance

NICOTINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1988-11-18

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2008
02 Jul
Bulk Ingredient NDC: 17205-612

Nonproprietary Name

Fluoxetine HCl

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried AG

Marketing Category

BULK INGREDIENT

17205-612

Substance

FLUOXETINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2008-07-02

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
16 Jun
Drug for Further Processing NDC: 17205-628

Nonproprietary Name

ZANUBRUTINIB

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried AG

Marketing Category

DRUG FOR FURTHER PROCESSING

17205-628

Substance

ZANUBRUTINIB

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

2023-06-16

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
14 Aug
Bulk Ingredient NDC: 17205-629

Nonproprietary Name

Lotilaner

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried AG

Marketing Category

BULK INGREDIENT

17205-629

Substance

LOTILANER

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-08-14

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1967
21 Mar
Bulk Ingredient NDC: 0792-0004

Nonproprietary Name

Phenobarbital Sodium

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried USA, LLC

Marketing Category

BULK INGREDIENT

0792-0004

Substance

PHENOBARBITAL SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

CIV

Start Marketing Date

1967-03-21

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1968
19 Apr
Bulk Ingredient NDC: 0792-0044

Nonproprietary Name

Pentobarbital Sodium

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried USA, LLC

Marketing Category

BULK INGREDIENT

0792-0044

Substance

PENTOBARBITAL SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

1968-04-19

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1968
19 Apr
Bulk Ingredient NDC: 0792-0045

Nonproprietary Name

Pentobarbital Sodium

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried USA, LLC

Marketing Category

BULK INGREDIENT

0792-0045

Substance

PENTOBARBITAL SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

1968-04-19

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2013
30 Jan
Bulk Ingredient NDC: 0792-0046

Nonproprietary Name

Ferric Citrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried USA, LLC

Marketing Category

BULK INGREDIENT

0792-0046

Substance

TETRAFERRIC TRICITRATE DECAHYDRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2013-01-30

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1967
23 Mar
Bulk Ingredient NDC: 0792-0099

Nonproprietary Name

Amobarbital Sodium

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried USA, LLC

Marketing Category

BULK INGREDIENT

0792-0099

Substance

AMOBARBITAL SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

1967-03-23

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
18 Dec
Bulk Ingredient NDC: 0792-0101

Nonproprietary Name

Methylphenidate Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried USA, LLC

Marketing Category

BULK INGREDIENT

0792-0101

Substance

METHYLPHENIDATE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2019-12-18

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1968
09 Apr
Bulk Ingredient NDC: 0792-0134

Nonproprietary Name

Butalbital

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried USA, LLC

Marketing Category

BULK INGREDIENT

0792-0134

Substance

BUTALBITAL

Product Type

BULK INGREDIENT

DEA Schedule

CIII

Start Marketing Date

1968-04-09

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1968
09 Apr
Bulk Ingredient NDC: 0792-0135

Nonproprietary Name

Butalbital

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried USA, LLC

Marketing Category

BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING

0792-0135

Substance

BUTALBITAL

Product Type

BULK INGREDIENT

DEA Schedule

CIII

Start Marketing Date

1968-04-09

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1979
09 Jan
Bulk Ingredient NDC: 0792-0344

Nonproprietary Name

Phentermine Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried USA, LLC

Marketing Category

BULK INGREDIENT

0792-0344

Substance

PHENTERMINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

CIV

Start Marketing Date

1979-01-09

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2015
15 Dec
Bulk Ingredient NDC: 0792-0345

Nonproprietary Name

Phentermine Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried USA, LLC

Marketing Category

BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING

0792-0345

Substance

PHENTERMINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

CIV

Start Marketing Date

2015-12-15

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1986
11 Mar
Bulk Ingredient NDC: 0792-0359

Nonproprietary Name

Methadone Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried USA, LLC

Marketing Category

BULK INGREDIENT

0792-0359

Substance

METHADONE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

1986-03-11

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2015
15 Dec
Bulk Ingredient NDC: 0792-0360

Nonproprietary Name

Methadone Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried USA, LLC

Marketing Category

BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING

0792-0360

Substance

METHADONE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2015-12-15

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1979
09 Jan
Bulk Ingredient NDC: 0792-0415

Nonproprietary Name

Phentermine Base

Dosage Form

LIQUID

Strength

1 kg/kg

Labeler

Siegfried USA, LLC

Marketing Category

BULK INGREDIENT

0792-0415

Substance

PHENTERMINE

Product Type

BULK INGREDIENT

DEA Schedule

CIV

Start Marketing Date

1979-01-09

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2006
26 May
Bulk Ingredient NDC: 0792-0543

Nonproprietary Name

Hydrocodone Bitartrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried USA, LLC

Marketing Category

BULK INGREDIENT

0792-0543

Substance

HYDROCODONE BITARTRATE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2006-05-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1998
21 Sep
Bulk Ingredient NDC: 0792-0619

Nonproprietary Name

Dexmethylphenidate Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried USA, LLC

Marketing Category

BULK INGREDIENT

0792-0619

Substance

DEXMETHYLPHENIDATE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

1998-09-21

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2011
16 Nov
Bulk Ingredient NDC: 0792-0630

Nonproprietary Name

Buprenorphine Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried USA, LLC

Marketing Category

BULK INGREDIENT

0792-0630

Substance

BUPRENORPHINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

CIII

Start Marketing Date

2011-11-16

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2015
27 Feb
Bulk Ingredient NDC: 0792-0631

Nonproprietary Name

Buprenorphine

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried USA, LLC

Marketing Category

BULK INGREDIENT

0792-0631

Substance

BUPRENORPHINE

Product Type

BULK INGREDIENT

DEA Schedule

CIII

Start Marketing Date

2015-02-27

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2008
01 Oct
Bulk Ingredient NDC: 0792-0632

Nonproprietary Name

Hydromorphone Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried USA, LLC

Marketing Category

BULK INGREDIENT

0792-0632

Substance

HYDROMORPHONE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2008-10-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2011
16 Nov
Bulk Ingredient NDC: 0792-0634

Nonproprietary Name

Buprenorphine Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried USA, LLC

Marketing Category

BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING

0792-0634

Substance

BUPRENORPHINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

CIII

Start Marketing Date

2011-11-16

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2008
01 May
Bulk Ingredient NDC: 0792-0636

Nonproprietary Name

Peramivir

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried USA, LLC

Marketing Category

BULK INGREDIENT

0792-0636

Substance

PERAMIVIR

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2008-05-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2007
29 Jan
Bulk Ingredient NDC: 0792-0644

Nonproprietary Name

Codeine Phosphate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried USA, LLC

Marketing Category

BULK INGREDIENT

0792-0644

Substance

CODEINE PHOSPHATE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2007-01-29

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2010
04 Feb
Bulk Ingredient NDC: 0792-2936

Nonproprietary Name

Oxycodone Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried USA, LLC

Marketing Category

BULK INGREDIENT

0792-2936

Substance

OXYCODONE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2010-02-04

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
02 Dec
Bulk Ingredient NDC: 0792-3936

Nonproprietary Name

Amphetamine Sulfate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried USA, LLC

Marketing Category

BULK INGREDIENT

0792-3936

Substance

AMPHETAMINE SULFATE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2022-12-02

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
17 Jul
Bulk Ingredient NDC: 0792-3937

Nonproprietary Name

Amphetamine Aspartate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried USA, LLC

Marketing Category

BULK INGREDIENT

0792-3937

Substance

AMPHETAMINE ASPARTATE MONOHYDRATE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2023-07-17

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
15 Aug
Bulk Ingredient NDC: 0792-3938

Nonproprietary Name

Dextroamphetamine Saccharate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried USA, LLC

Marketing Category

BULK INGREDIENT

0792-3938

Substance

DEXTROAMPHETAMINE SACCHARATE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2023-08-15

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
22 Nov
Bulk Ingredient NDC: 0792-3939

Nonproprietary Name

Dextroamphetamine Sulfate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried USA, LLC

Marketing Category

BULK INGREDIENT

0792-3939

Substance

DEXTROAMPHETAMINE SULFATE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2023-11-22

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2024
26 Jul
Bulk Ingredient NDC: 0792-3940

Nonproprietary Name

Inc-15-Ruxo Phosphate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried USA, LLC

Marketing Category

BULK INGREDIENT

0792-3940

Substance

RUXOLITINIB PHOSPHATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-07-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2024
06 Nov
Bulk Ingredient NDC: 0792-3941

Nonproprietary Name

Naltrexone Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried USA, LLC

Marketing Category

BULK INGREDIENT

0792-3941

Substance

NALTREXONE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-11-06

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2011
30 May
Bulk Ingredient NDC: 0792-4356

Nonproprietary Name

Sodium Oxybate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried USA, LLC

Marketing Category

BULK INGREDIENT

0792-4356

Substance

SODIUM OXYBATE

Product Type

BULK INGREDIENT

DEA Schedule

CI

Start Marketing Date

2011-05-30

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
13 Dec
Bulk Ingredient NDC: 0792-5671

Nonproprietary Name

Tapentadol hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried USA, LLC

Marketing Category

BULK INGREDIENT

0792-5671

Substance

TAPENTADOL HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2022-12-13

End Marketing Date

-

Listing Record Certified Through

2026-12-31

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NDC Type Breakdown
54 total
  • Bulk Ingredient
  • Drug for Further Processing
Official Source

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

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

NDC

17205-096

Nonproprietary Name

Topiramate

Labeler

Siegfried AG

Dosage Form

POWDER

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

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