Moehs Iberica
NDC Database

Moehs Iberica

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 33
  • Latest Marketing Date 2025-10-02
  • Data Source FDA
  • First Marketing Date 2009-07-21
Company Overview

Company

Moehs Iberica

Country

Spain

Social Profiles

LinkedIn X / Twitter
Company Snapshot

Moehs Iberica

Pol. Ind. Cova Solera, c/ Roma, 8-12 08191 Rubí, Barcelona

Spain

moehs.com/ info@moehs.es View on Map
NDC Records ( 33 records )
2009
28 Oct
Bulk Ingredient NDC: 68294-0001

Nonproprietary Name

Fenofibrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Coprima SL

Marketing Category

BULK INGREDIENT

68294-0001

Substance

FENOFIBRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-10-28

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2009
28 Oct
Bulk Ingredient NDC: 68294-0002

Nonproprietary Name

Fenofibrate Micronized

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Coprima SL

Marketing Category

BULK INGREDIENT

68294-0002

Substance

FENOFIBRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-10-28

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2009
21 Jul
Bulk Ingredient NDC: 68294-0003

Nonproprietary Name

Choline Fenofibrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Coprima SL

Marketing Category

BULK INGREDIENT

68294-0003

Substance

CHOLINE FENOFIBRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-07-21

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2013
05 Apr
Bulk Ingredient NDC: 68294-0005

Nonproprietary Name

CARVEDILOL

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

COPRIMA SL

Marketing Category

BULK INGREDIENT

68294-0005

Substance

CARVEDILOL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2013-04-05

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2016
20 Jul
Bulk Ingredient NDC: 68294-0006

Nonproprietary Name

Celiprolol HCI

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Coprima SL

Marketing Category

BULK INGREDIENT

68294-0006

Substance

CELIPROLOL HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2016-07-20

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
01 Jan
Bulk Ingredient NDC: 68294-0008

Nonproprietary Name

Pyrantel Pamoate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Coprima SL

Marketing Category

BULK INGREDIENT

68294-0008

Substance

PYRANTEL PAMOATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2010
23 Jul
Bulk Ingredient NDC: 68069-0005

Nonproprietary Name

Pantoprazole Sodium Sesquihydrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Moehs Cantabra SL

Marketing Category

BULK INGREDIENT

68069-0005

Substance

PANTOPRAZOLE SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2010-07-23

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2009
28 Oct
Bulk Ingredient NDC: 68069-0006

Nonproprietary Name

Quetiapine Fumarate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Moehs Cantabra SL

Marketing Category

BULK INGREDIENT

68069-0006

Substance

QUETIAPINE FUMARATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-10-28

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2009
28 Oct
Bulk Ingredient NDC: 68069-0008

Nonproprietary Name

Amantadine Sulphate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Moehs Cantabra SL

Marketing Category

BULK INGREDIENT

68069-0008

Substance

AMANTADINE SULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-10-28

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2009
28 Oct
Bulk Ingredient NDC: 68069-0009

Nonproprietary Name

Acebutolol Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Moehs Cantabra SL

Marketing Category

BULK INGREDIENT

68069-0009

Substance

ACEBUTOLOL HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-10-28

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
23 Jul
Bulk Ingredient NDC: 68069-0010

Nonproprietary Name

Articaine HCl

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Moehs Cantabra SL

Marketing Category

BULK INGREDIENT

68069-0010

Substance

ARTICAINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-07-23

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2009
29 Sep
Bulk Ingredient NDC: 52932-0701

Nonproprietary Name

LIDOCAINE HYDROCHLORIDE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Moehs Catalana SL

Marketing Category

BULK INGREDIENT

52932-0701

Substance

LIDOCAINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-09-29

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2009
29 Sep
Bulk Ingredient NDC: 52932-0702

Nonproprietary Name

LIDOCAINE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Moehs Catalana SL

Marketing Category

BULK INGREDIENT

52932-0702

Substance

LIDOCAINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-09-29

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2009
28 Oct
Bulk Ingredient NDC: 52932-0703

Nonproprietary Name

Triamterene

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Moehs Catalana SL

Marketing Category

BULK INGREDIENT

52932-0703

Substance

TRIAMTERENE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-10-28

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2009
29 Sep
Bulk Ingredient NDC: 52932-0704

Nonproprietary Name

ACETYLCYSTEINE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Moehs Catalana SL

Marketing Category

BULK INGREDIENT

52932-0704

Substance

ACETYLCYSTEINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-09-29

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2009
29 Sep
Bulk Ingredient NDC: 52932-0707

Nonproprietary Name

AMANTADINE HYDROCHLORIDE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Moehs Catalana SL

Marketing Category

BULK INGREDIENT

52932-0707

Substance

AMANTADINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-09-29

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2009
29 Sep
Bulk Ingredient NDC: 52932-0710

Nonproprietary Name

METOPROLOL TARTRATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Moehs Catalana SL

Marketing Category

BULK INGREDIENT

52932-0710

Substance

METOPROLOL TARTRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-09-29

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2009
29 Sep
Bulk Ingredient NDC: 52932-0711

Nonproprietary Name

NIFEDIPINE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Moehs Catalana SL

Marketing Category

BULK INGREDIENT

52932-0711

Substance

NIFEDIPINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-09-29

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2009
29 Sep
Bulk Ingredient NDC: 52932-0713

Nonproprietary Name

METOPROLOL SUCCINATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Moehs Catalana SL

Marketing Category

BULK INGREDIENT

52932-0713

Substance

METOPROLOL SUCCINATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-09-29

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2009
29 Sep
Bulk Ingredient NDC: 52932-0714

Nonproprietary Name

PYRANTEL PAMOATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Moehs Catalana SL

Marketing Category

BULK INGREDIENT

52932-0714

Substance

PYRANTEL PAMOATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-09-29

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2009
28 Oct
Bulk Ingredient NDC: 52932-0715

Nonproprietary Name

SOTALOL HYDROCHLORIDE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Moehs Catalana SL

Marketing Category

BULK INGREDIENT

52932-0715

Substance

SOTALOL HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-10-28

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2009
29 Sep
Bulk Ingredient NDC: 52932-0720

Nonproprietary Name

BISOPROLOL FUMARATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Moehs Catalana SL

Marketing Category

BULK INGREDIENT

52932-0720

Substance

BISOPROLOL FUMARATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-09-29

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2009
29 Sep
Bulk Ingredient NDC: 52932-0721

Nonproprietary Name

METOPROLOL TARTRATE DS/IP

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Moehs Catalana SL

Marketing Category

BULK INGREDIENT

52932-0721

Substance

METOPROLOL TARTRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-09-29

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2010
23 Jul
Bulk Ingredient NDC: 52932-0723

Nonproprietary Name

AMLODIPINE BESYLATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Moehs Catalana SL

Marketing Category

BULK INGREDIENT

52932-0723

Substance

AMLODIPINE BESYLATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2010-07-23

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2015
02 Feb
Bulk Ingredient NDC: 52932-0726

Nonproprietary Name

CARVEDILOL

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Moehs Catalana SL

Marketing Category

BULK INGREDIENT

52932-0726

Substance

CARVEDILOL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2015-02-02

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2009
28 Oct
Bulk Ingredient NDC: 52932-0727

Nonproprietary Name

Sumatriptan Succinate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Moehs Catalana SL

Marketing Category

BULK INGREDIENT

52932-0727

Substance

SUMATRIPTAN SUCCINATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-10-28

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2009
29 Sep
Bulk Ingredient NDC: 52932-0729

Nonproprietary Name

BUPIVACAINE HYDROCHLORIDE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Moehs Catalana SL

Marketing Category

BULK INGREDIENT

52932-0729

Substance

BUPIVACAINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-09-29

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2009
29 Sep
Bulk Ingredient NDC: 52932-0730

Nonproprietary Name

LANSOPRAZOLE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Moehs Catalana SL

Marketing Category

BULK INGREDIENT

52932-0730

Substance

LANSOPRAZOLE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-09-29

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2009
29 Sep
Bulk Ingredient NDC: 52932-0731

Nonproprietary Name

MEPIVACAINE HYDROCHLORIDE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Moehs Catalana SL

Marketing Category

BULK INGREDIENT

52932-0731

Substance

MEPIVACAINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-09-29

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2009
28 Oct
Bulk Ingredient NDC: 52932-0733

Nonproprietary Name

SUMATRIPTAN

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Moehs Catalana SL

Marketing Category

BULK INGREDIENT

52932-0733

Substance

SUMATRIPTAN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-10-28

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
01 Jul
Bulk Ingredient NDC: 81912-0001

Nonproprietary Name

Dexmedetomidine HCl

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Moehs Iberica SL

Marketing Category

BULK INGREDIENT

81912-0001

Substance

DEXMEDETOMIDINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-07-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
22 Sep
Bulk Ingredient NDC: 81912-0002

Nonproprietary Name

Rimegepant Hemisulfate Sesquihydrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Moehs Iberica SL

Marketing Category

BULK INGREDIENT

81912-0002

Substance

RIMEGEPANT SULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-09-22

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
02 Oct
Bulk Ingredient NDC: 81912-0003

Nonproprietary Name

Mavacamten

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Moehs Iberica SL

Marketing Category

BULK INGREDIENT

81912-0003

Substance

MAVACAMTEN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-10-02

End Marketing Date

-

Listing Record Certified Through

2026-12-31

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NDC Type Breakdown
33 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

68294-0001

Nonproprietary Name

Fenofibrate

Labeler

Coprima SL

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.

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