"76420-151-30" National Drug Code (NDC)

Finasteride 30 TABLET, FILM COATED in 1 BOTTLE (76420-151-30)
(Asclemed USA, Inc.)

NDC Code76420-151-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE (76420-151-30)
Product NDC76420-151
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFinasteride
Non-Proprietary NameFinasteride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20131105
Marketing Category NameANDA
Application NumberANDA203687
ManufacturerAsclemed USA, Inc.
Substance NameFINASTERIDE
Strength1
Strength Unitmg/1
Pharmacy Classes5-alpha Reductase Inhibitor [EPC], 5-alpha Reductase Inhibitors [MoA]

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