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Clopidogrel - 50436-9986-1 - (Clopidogrel Bisulfate)

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Drug Information of Clopidogrel

Product NDC: 50436-9986
Proprietary Name: Clopidogrel
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

Product NDC: 50436-9986
Labeler Name: Unit Dose Services
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090540
Marketing Category: ANDA
Start Marketing Date: 20120517

Package Information of Clopidogrel

Package NDC: 50436-9986-1
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (50436-9986-1)

NDC Information of Clopidogrel

NDC Code 50436-9986-1
Proprietary Name Clopidogrel
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (50436-9986-1)
Product NDC 50436-9986
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 Unit Dose Services
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


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