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"50268-323-15" National Drug Code (NDC)

Finasteride 50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-323-15) > 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-323-11)
(AvPAK)

NDC Code50268-323-15
Package Description50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-323-15) > 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-323-11)
Product NDC50268-323
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFinasteride
Non-Proprietary NameFinasteride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20110321
Marketing Category NameANDA
Application NumberANDA077914
ManufacturerAvPAK
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/50268-323-15





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