"68788-6875-3" National Drug Code (NDC)

Finasteride 30 TABLET, FILM COATED in 1 BOTTLE (68788-6875-3)
(Preferred Pharmaceuticals Inc.)

NDC Code68788-6875-3
Package Description30 TABLET, FILM COATED in 1 BOTTLE (68788-6875-3)
Product NDC68788-6875
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFinasteride
Non-Proprietary NameFinasteride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20170123
Marketing Category NameANDA
Application NumberANDA203687
ManufacturerPreferred Pharmaceuticals Inc.
Substance NameFINASTERIDE
Strength1
Strength Unitmg/1
Pharmacy Classes5-alpha Reductase Inhibitor [EPC], 5-alpha Reductase Inhibitors [MoA]

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