Unither Pharmaceuticals
NDC Database

Unither Pharmaceuticals

NDC Database

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

Drug for Further Processing
  • Total Records 2
  • Latest Marketing Date 2024-04-16
  • Data Source FDA
  • First Marketing Date 2013-11-11
Company Overview

Company

Unither Pharmaceuticals

Country

France

Social Profiles

LinkedIn X / Twitter
Company Snapshot

Unither Pharmaceuticals

3-5 rue Saint Georges, 75009, Paris

France

www.unither-pharma.com/ unither@unither-pharma.com View on Map
NDC Records ( 2 records )
2024
16 Apr
Drug for Further Processing NDC: 43014-0538

Nonproprietary Name

BRIMONIDINE TARTRATE

Dosage Form

SOLUTION/ DROPS

Strength

0.25 mg/mL

Labeler

Laboratoire Unither

Marketing Category

DRUG FOR FURTHER PROCESSING

43014-0538

Substance

BRIMONIDINE TARTRATE

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

2024-04-16

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2013
11 Nov
Drug for Further Processing NDC: 53014-151

Nonproprietary Name

carboxymethylcellulose sodium, unspecified

Dosage Form

SOLUTION, GEL FORMING / DROPS

Strength

0.5 g/100mL

Labeler

Unither Manufacturing LLC

Marketing Category

DRUG FOR FURTHER PROCESSING

53014-151

Substance

CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

2013-11-11

End Marketing Date

-

Listing Record Certified Through

2026-12-31

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NDC Type Breakdown
2 total
  • 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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NDC Record Details Preview

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

NDC

43014-0538

Nonproprietary Name

BRIMONIDINE TARTRATE

Labeler

Laboratoire Unither

Dosage Form

SOLUTION/ DROPS

FDA NDC Data

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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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