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"68071-4808-3" National Drug Code (NDC)

Finasteride 30 TABLET, FILM COATED in 1 BOTTLE (68071-4808-3)
(NuCare Pharmaceuticals,Inc.)

NDC Code68071-4808-3
Package Description30 TABLET, FILM COATED in 1 BOTTLE (68071-4808-3)
Product NDC68071-4808
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFinasteride
Non-Proprietary NameFinasteride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20140920
Marketing Category NameANDA
Application NumberANDA203687
ManufacturerNuCare Pharmaceuticals,Inc.
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/68071-4808-3





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