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"0006-0071-07" National Drug Code (NDC)

Propecia 1 BLISTER PACK in 1 CARTON (0006-0071-07) > 7 TABLET, FILM COATED in 1 BLISTER PACK
(Merck Sharp & Dohme Corp.)

NDC Code0006-0071-07
Package Description1 BLISTER PACK in 1 CARTON (0006-0071-07) > 7 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC0006-0071
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePropecia
Non-Proprietary NameFinasteride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date19971219
Marketing Category NameNDA
Application NumberNDA020788
ManufacturerMerck Sharp & Dohme Corp.
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/0006-0071-07





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