Par Pharmaceutical
NDC Database

Par Pharmaceutical

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 8
  • Latest Marketing Date 2023-03-07
  • Data Source FDA
  • First Marketing Date 2015-09-15
Company Overview

Company

Par Pharmaceutical

Country

U.S.A

Website

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Company Snapshot

Par Pharmaceutical

300 Tice BoulevardWoodcliff Lake, NJ 07677

U.S.A

www.parpharm.com/ View on Map
NDC Records ( 8 records )
2015
15 Sep
Bulk Ingredient NDC: 70054-002

Nonproprietary Name

COLCHICINE

Dosage Form

POWDER

Strength

10 kg/10kg

Labeler

Par Active Technologies Private Limited

Marketing Category

BULK INGREDIENT

70054-002

Substance

COLCHICINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2015-09-15

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2015
15 Sep
Bulk Ingredient NDC: 70054-004

Nonproprietary Name

Midodrine Hydrochloride

Dosage Form

POWDER

Strength

20 kg/20kg

Labeler

Par Active Technologies Private Limited

Marketing Category

BULK INGREDIENT

70054-004

Substance

MIDODRINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2015-09-15

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2015
15 Sep
Bulk Ingredient NDC: 70054-006

Nonproprietary Name

ZAFIRLUKAST

Dosage Form

POWDER

Strength

30 kg/30kg

Labeler

Par Active Technologies Private Limited

Marketing Category

BULK INGREDIENT

70054-006

Substance

ZAFIRLUKAST

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2015-09-15

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2018
17 Dec
Bulk Ingredient NDC: 70054-021

Nonproprietary Name

Mafenide Acetate

Dosage Form

POWDER

Strength

5 kg/5kg

Labeler

Par Active Technologies Private Limited

Marketing Category

BULK INGREDIENT

70054-021

Substance

MAFENIDE ACETATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2018-12-17

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2016
29 Jul
Bulk Ingredient NDC: 70054-022

Nonproprietary Name

Varenicline Tartrate

Dosage Form

POWDER

Strength

6 kg/6kg

Labeler

Par Active Technologies Private Limited

Marketing Category

BULK INGREDIENT

70054-022

Substance

VARENICLINE TARTRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2016-07-29

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2018
17 Dec
Bulk Ingredient NDC: 70054-029

Nonproprietary Name

Sodium Phenylbutyrate

Dosage Form

POWDER

Strength

5 kg/5kg

Labeler

Par Active Technologies Private Limited

Marketing Category

BULK INGREDIENT

70054-029

Substance

SODIUM PHENYLBUTYRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2018-12-17

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2018
17 Dec
Bulk Ingredient NDC: 70054-030

Nonproprietary Name

Benztropine Mesylate

Dosage Form

POWDER

Strength

5 kg/5kg

Labeler

Par Active Technologies Private Limited

Marketing Category

BULK INGREDIENT

70054-030

Substance

BENZTROPINE MESYLATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2018-12-17

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
07 Mar
Bulk Ingredient NDC: 70054-036

Nonproprietary Name

Bismuth Subcitrate Potassium

Dosage Form

POWDER

Strength

16 kg/16kg

Labeler

Par Active Technologies Private Limited

Marketing Category

BULK INGREDIENT

70054-036

Substance

BISMUTH SUBCITRATE POTASSIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-03-07

End Marketing Date

-

Listing Record Certified Through

2026-12-31

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NDC Type Breakdown
8 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

70054-002

Nonproprietary Name

COLCHICINE

Labeler

Par Active Technologies Private Limited

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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