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Clopidogrel Bisulfate - 49349-990-02 - (Clopidogrel Bisulfate)

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Drug Information of Clopidogrel Bisulfate

Product NDC: 49349-990
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: 49349-990
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090844
Marketing Category: ANDA
Start Marketing Date: 20130220

Package Information of Clopidogrel Bisulfate

Package NDC: 49349-990-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-990-02)

NDC Information of Clopidogrel Bisulfate

NDC Code 49349-990-02
Proprietary Name Clopidogrel Bisulfate
Package Description 30 TABLET in 1 BLISTER PACK (49349-990-02)
Product NDC 49349-990
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clopidogrel Bisulfate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130220
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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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