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"70518-1383-0" National Drug Code (NDC)

Clopidogrel 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1383-0)
(REMEDYREPACK INC.)

NDC Code70518-1383-0
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1383-0)
Product NDC70518-1383
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameClopidogrel
Non-Proprietary NameClopidogrel Bisulfate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20180823
Marketing Category NameANDA
Application NumberANDA076274
ManufacturerREMEDYREPACK 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/70518-1383-0





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