"68071-2620-9" National Drug Code (NDC)

Finasteride 90 TABLET, COATED in 1 BOTTLE (68071-2620-9)
(NuCare Pharmaceuticals,Inc.)

NDC Code68071-2620-9
Package Description90 TABLET, COATED in 1 BOTTLE (68071-2620-9)
Product NDC68071-2620
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFinasteride
Non-Proprietary NameFinasteride
Dosage FormTABLET, COATED
UsageORAL
Start Marketing Date20170106
Marketing Category NameANDA
Application NumberANDA207750
ManufacturerNuCare Pharmaceuticals,Inc.
Substance NameFINASTERIDE
Strength1
Strength Unitmg/1
Pharmacy Classes5-alpha Reductase Inhibitor [EPC], 5-alpha Reductase Inhibitors [MoA]

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