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"70710-1417-0" National Drug Code (NDC)

Clopidogrel 1000 TABLET, FILM COATED in 1 BOTTLE (70710-1417-0)
(Zydus Pharmaceuticals (USA) Inc.)

NDC Code70710-1417-0
Package Description1000 TABLET, FILM COATED in 1 BOTTLE (70710-1417-0)
Product NDC70710-1417
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameClopidogrel
Non-Proprietary NameClopidogrel
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20170208
Marketing Category NameANDA
Application NumberANDA201686
ManufacturerZydus Pharmaceuticals (USA) Inc.
Substance NameCLOPIDOGREL BISULFATE
Strength75
Strength Unitmg/1
Pharmacy ClassesDecreased Platelet Aggregation [PE],P2Y12 Platelet Inhibitor [EPC],P2Y12 Receptor Antagonists [MoA],Cytochrome P450 2C8 Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70710-1417-0





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