"31722-525-05" National Drug Code (NDC)

Finasteride 500 TABLET, FILM COATED in 1 BOTTLE (31722-525-05)
(Camber Pharmaceuticals, Inc.)

NDC Code31722-525-05
Package Description500 TABLET, FILM COATED in 1 BOTTLE (31722-525-05)
Product NDC31722-525
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFinasteride
Non-Proprietary NameFinasteride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20150613
Marketing Category NameANDA
Application NumberANDA090061
ManufacturerCamber Pharmaceuticals, Inc.
Substance NameFINASTERIDE
Strength5
Strength Unitmg/1
Pharmacy Classes5-alpha Reductase Inhibitor [EPC], 5-alpha Reductase Inhibitors [MoA]

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