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"48792-7821-1" National Drug Code (NDC)

Prasugrel 30 TABLET, FILM COATED in 1 BOTTLE (48792-7821-1)
(Sunshine Lake Pharma Co., Ltd.)

NDC Code48792-7821-1
Package Description30 TABLET, FILM COATED in 1 BOTTLE (48792-7821-1)
Product NDC48792-7821
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePrasugrel
Non-Proprietary NamePrasugrel Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190130
Marketing Category NameANDA
Application NumberANDA206021
ManufacturerSunshine Lake Pharma Co., Ltd.
Substance NamePRASUGREL HYDROCHLORIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesDecreased Platelet Aggregation [PE],P2Y12 Platelet Inhibitor [EPC],P2Y12 Receptor Antagonists [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/48792-7821-1





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