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clopidogrel bisulfate - 60429-301-10 - (clopidogrel bisulfate)

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Drug Information of clopidogrel bisulfate

Product NDC: 60429-301
Proprietary Name: clopidogrel bisulfate
Non Proprietary Name: clopidogrel bisulfate
Active Ingredient(s): 75    mg/1 & nbsp;   clopidogrel bisulfate
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of clopidogrel bisulfate

Product NDC: 60429-301
Labeler Name: Golden State Medical Supply, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076274
Marketing Category: ANDA
Start Marketing Date: 20120517

Package Information of clopidogrel bisulfate

Package NDC: 60429-301-10
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (60429-301-10)

NDC Information of clopidogrel bisulfate

NDC Code 60429-301-10
Proprietary Name clopidogrel bisulfate
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (60429-301-10)
Product NDC 60429-301
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name clopidogrel bisulfate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120517
Marketing Category Name ANDA
Labeler Name Golden State Medical Supply, Inc.
Substance Name CLOPIDOGREL BISULFATE
Strength Number 75
Strength Unit mg/1
Pharmaceutical Classes Decreased Platelet Aggregation [PE],P2Y12 Platelet Inhibitor [EPC],P2Y12 Receptor Antagonists [MoA]

Complete Information of clopidogrel bisulfate


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