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"71335-0235-5" National Drug Code (NDC)

Finasteride 180 TABLET, FILM COATED in 1 BOTTLE (71335-0235-5)
(Bryant Ranch Prepack)

NDC Code71335-0235-5
Package Description180 TABLET, FILM COATED in 1 BOTTLE (71335-0235-5)
Product NDC71335-0235
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFinasteride
Non-Proprietary NameFinasteride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20131108
Marketing Category NameANDA
Application NumberANDA091643
ManufacturerBryant Ranch Prepack
Substance NameFINASTERIDE
Strength1
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/71335-0235-5





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