Clopidogrel Bisulfate Drug For Further Processing - NDC Database

NDC Database
3 labelers
Clopidogrel Bisulfate Drug For Further Processing

Clopidogrel Bisulfate Drug For Further Processing

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

DRUG FOR FURTHER PROCESSING
Last Marketing Date
2012-05-17
Data Source
FDA
First Marketing Date
2012-02-27
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NDC Records Timeline (3 records)
Clear
2012
17 May
Apotex Corp.
DRUG FOR FURTHER PROCESSING

NDC

60505-3992

Labeler

Apotex Corp.

Nonproprietary Name

clopidogrel bisulfate

Marketing Category

DRUG FOR FURTHER PROCESSING

Dosage Form

TABLET, FILM COATED

Strength

75 mg/1

Start Marketing: 2012-05-17

Substance

CLOPIDOGREL BISULFATE

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

2012-05-17

End Marketing Date

-

Listing / Certification

2026-12-31

2012
27 Feb
Sanofi Winthrop Industrie
DRUG FOR FURTHER PROCESSING

NDC

53360-1171

Labeler

Sanofi Winthrop Industrie

Nonproprietary Name

clopidogrel bisulfate

Marketing Category

DRUG FOR FURTHER PROCESSING

Dosage Form

TABLET, FILM COATED

Strength

75 mg/1

Start Marketing: 2012-02-27

Substance

CLOPIDOGREL BISULFATE

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

2012-02-27

End Marketing Date

-

Listing / Certification

2026-12-31

2012
17 May
DRUG FOR FURTHER PROCESSING

NDC

65862-357

Labeler

Aurobindo Pharma Limited

Nonproprietary Name

Clopidogrel Bisulfate

Marketing Category

DRUG FOR FURTHER PROCESSING

Dosage Form

TABLET, FILM COATED

Strength

75 mg/1

Start Marketing: 2012-05-17

Substance

CLOPIDOGREL BISULFATE

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

2012-05-17

End Marketing Date

-

Listing / Certification

2026-12-31

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Product Type Breakdown
3 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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Substance

CLOPIDOGREL BISULFATE

Identifiers

NDC: 60505-3992
DEA Schedule:

Official FDA Data

Based on publicly available FDA NDC information

National Drug Code

Structured NDC product information

Product Information

Drug, labeler and marketing 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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