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Clopidogrel bisulfate - 68788-9785-9 - (Clopidogrel bisulfate)

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Drug Information of Clopidogrel bisulfate

Product NDC: 68788-9785
Proprietary Name: Clopidogrel bisulfate
Non Proprietary Name: Clopidogrel bisulfate
Active Ingredient(s): 300    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: 68788-9785
Labeler Name: Preferred Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076273
Marketing Category: ANDA
Start Marketing Date: 20120517

Package Information of Clopidogrel bisulfate

Package NDC: 68788-9785-9
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (68788-9785-9)

NDC Information of Clopidogrel bisulfate

NDC Code 68788-9785-9
Proprietary Name Clopidogrel bisulfate
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (68788-9785-9)
Product NDC 68788-9785
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 Preferred Pharmaceuticals, Inc.
Substance Name CLOPIDOGREL BISULFATE
Strength Number 300
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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