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"71335-1530-5" National Drug Code (NDC)

Finasteride 500 TABLET, FILM COATED in 1 BOTTLE (71335-1530-5)
(Bryant Ranch Prepack)

NDC Code71335-1530-5
Package Description500 TABLET, FILM COATED in 1 BOTTLE (71335-1530-5)
Product NDC71335-1530
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFinasteride
Non-Proprietary NameFinasteride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20071030
Marketing Category NameANDA
Application NumberANDA078341
ManufacturerBryant Ranch Prepack
Substance NameFINASTERIDE
Strength5
Strength Unitmg/1
Pharmacy Classes5-alpha Reductase Inhibitor [EPC], 5-alpha Reductase Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71335-1530-5





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