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Clopidogrel Bisulfate - 43063-371-90 - (Clopidogrel Bisulfate)

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Drug Information of Clopidogrel Bisulfate

Product NDC: 43063-371
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
Coding System: National Drug Codes(NDC)

Labeler Information of Clopidogrel Bisulfate

Product NDC: 43063-371
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090844
Marketing Category: ANDA
Start Marketing Date: 20120517

Package Information of Clopidogrel Bisulfate

Package NDC: 43063-371-90
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC (43063-371-90)

NDC Information of Clopidogrel Bisulfate

NDC Code 43063-371-90
Proprietary Name Clopidogrel Bisulfate
Package Description 90 TABLET in 1 BOTTLE, PLASTIC (43063-371-90)
Product NDC 43063-371
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clopidogrel Bisulfate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120517
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, 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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