Arevipharma
NDC Database

Arevipharma

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 12
  • Latest Marketing Date 2026-05-28
  • Data Source FDA
  • First Marketing Date 2010-11-23
Company Overview

Company

Arevipharma

Country

Germany

Website

Visit Website

Email

Kerstin.dreissig@arevipharma.com

Social Profiles

LinkedIn
Company Snapshot

Arevipharma

Meißner Str. 35 01445 Radebeul

Germany

www.arevipharma.com/ Kerstin.dreissig@arevipharma.com View on Map
NDC Records ( 12 records )
2010
23 Nov
Bulk Ingredient NDC: 10920-571

Nonproprietary Name

Bisoprolol fumarate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Arevipharma GmbH

Marketing Category

BULK INGREDIENT

10920-571

Substance

BISOPROLOL FUMARATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2010-11-23

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2011
11 Jan
Bulk Ingredient NDC: 10920-582

Nonproprietary Name

Imepitoin

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Arevipharma GmbH

Marketing Category

BULK INGREDIENT

10920-582

Substance

IMEPITOIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2011-01-11

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2011
02 Mar
Bulk Ingredient NDC: 10920-590

Nonproprietary Name

Buprenorphine hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Arevipharma GmbH

Marketing Category

BULK INGREDIENT

10920-590

Substance

BUPRENORPHINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

CIII

Start Marketing Date

2011-03-02

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
30 Jul
Bulk Ingredient NDC: 10920-593

Nonproprietary Name

Buprenorphine

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Arevipharma GmbH

Marketing Category

BULK INGREDIENT

10920-593

Substance

BUPRENORPHINE

Product Type

BULK INGREDIENT

DEA Schedule

CIII

Start Marketing Date

2012-07-30

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2013
09 Dec
Bulk Ingredient NDC: 10920-597

Nonproprietary Name

Ketamine Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Arevipharma GmbH

Marketing Category

BULK INGREDIENT

10920-597

Substance

KETAMINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

CIII

Start Marketing Date

2013-12-09

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2013
17 Dec
Bulk Ingredient NDC: 10920-598

Nonproprietary Name

Dimethyl Fumarate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Arevipharma GmbH

Marketing Category

BULK INGREDIENT

10920-598

Substance

DIMETHYL FUMARATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2013-12-17

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2014
12 May
Bulk Ingredient NDC: 10920-600

Nonproprietary Name

Diethylpropion Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Arevipharma GmbH

Marketing Category

BULK INGREDIENT

10920-600

Substance

DIETHYLPROPION HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

CIV

Start Marketing Date

2014-05-12

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2017
25 Oct
Bulk Ingredient NDC: 10920-601

Nonproprietary Name

Doxapram hydrochloride monohydrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Arevipharma GmbH

Marketing Category

BULK INGREDIENT

10920-601

Substance

DOXAPRAM HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2017-10-25

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
12 Jan
Bulk Ingredient NDC: 10920-700

Nonproprietary Name

Esketamine Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Arevipharma GmbH

Marketing Category

BULK INGREDIENT

10920-700

Substance

ESKETAMINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

CIII

Start Marketing Date

2022-01-12

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
13 Jan
Bulk Ingredient NDC: 10920-701

Nonproprietary Name

Arketamine Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Arevipharma GmbH

Marketing Category

BULK INGREDIENT

10920-701

Substance

KETAMINE HYDROCHLORIDE, (R)-

Product Type

BULK INGREDIENT

DEA Schedule

CIII

Start Marketing Date

2022-01-13

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
03 Feb
Bulk Ingredient NDC: 10920-702

Nonproprietary Name

Naltrexone

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Arevipharma GmbH

Marketing Category

BULK INGREDIENT

10920-702

Substance

NALTREXONE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-02-03

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2026
28 May
Bulk Ingredient NDC: 10920-703

Nonproprietary Name

Remifentanil Hydrochloride

Dosage Form

POWDER

Strength

100 kg/100kg

Labeler

Arevipharma GmbH

Marketing Category

BULK INGREDIENT

10920-703

Substance

REMIFENTANIL HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2026-05-28

End Marketing Date

-

Listing Record Certified Through

2027-12-31

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NDC Type Breakdown
12 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

10920-571

Nonproprietary Name

Bisoprolol fumarate

Labeler

Arevipharma GmbH

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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