ChemPacific Corp
NDC Database

ChemPacific Corp

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 5
  • Latest Marketing Date 2025-04-28
  • Data Source FDA
  • First Marketing Date 2003-01-09
Company Overview

Company

ChemPacific Corp

Country

U.S.A

Website

Visit Website

Email

sales@chempacific.com

Social Profiles

Company Snapshot

ChemPacific Corp

Chempacific Corp, 6200 Seaforth Street, Baltimore, MD 21224

U.S.A

www.chempacific.com/ sales@chempacific.com View on Map
NDC Records ( 5 records )
2003
09 Jan
Bulk Ingredient NDC: 66300-001

Nonproprietary Name

Norepinephrine Bitartrate

Dosage Form

POWDER

Strength

1 g/g

Labeler

ChemPacific Corporation

Marketing Category

BULK INGREDIENT

66300-001

Substance

NOREPINEPHRINE BITARTRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2003-01-09

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2010
12 Oct
Bulk Ingredient NDC: 59981-016

Nonproprietary Name

Melphalan Hydrochloride

Dosage Form

POWDER

Strength

1 g/g

Labeler

Zhejiang ChemPacific Corporation

Marketing Category

BULK INGREDIENT

59981-016

Substance

MELPHALAN HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2010-10-12

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2011
05 Aug
Bulk Ingredient NDC: 59981-023

Nonproprietary Name

Phenoxybenzamine Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Zhejiang ChemPacific Corporation

Marketing Category

BULK INGREDIENT

59981-023

Substance

PHENOXYBENZAMINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2011-08-05

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2016
15 Mar
Bulk Ingredient NDC: 59981-034

Nonproprietary Name

CARMUSTINE

Dosage Form

POWDER

Strength

1 g/g

Labeler

Zhejiang ChemPacific Corporation

Marketing Category

BULK INGREDIENT

59981-034

Substance

CARMUSTINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2016-03-15

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
28 Apr
Bulk Ingredient NDC: 59981-052

Nonproprietary Name

Floxuridine

Dosage Form

POWDER

Strength

1 g/g

Labeler

Zhejiang ChemPacific Corporation

Marketing Category

BULK INGREDIENT

59981-052

Substance

FLOXURIDINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-04-28

End Marketing Date

-

Listing Record Certified Through

2026-12-31

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NDC Type Breakdown
5 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).

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NDC Record Details Preview

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

NDC

66300-001

Nonproprietary Name

Norepinephrine Bitartrate

Labeler

ChemPacific Corporation

Dosage Form

POWDER

FDA NDC Data

National Drug Code information

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Data maintained from official sources

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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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