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"68382-074-30" National Drug Code (NDC)

Finasteride 10 BLISTER PACK in 1 CARTON (68382-074-30) > 10 TABLET, FILM COATED in 1 BLISTER PACK
(Zydus Pharmaceuticals (USA) Inc.)

NDC Code68382-074-30
Package Description10 BLISTER PACK in 1 CARTON (68382-074-30) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC68382-074
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFinasteride
Non-Proprietary NameFinasteride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20171205
Marketing Category NameANDA
Application NumberANDA078900
ManufacturerZydus Pharmaceuticals (USA) Inc.
Substance NameFINASTERIDE
Strength5
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/68382-074-30





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