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"68084-919-21" National Drug Code (NDC)

Finasteride 30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-919-21) > 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-919-11)
(American Health Packaging)

NDC Code68084-919-21
Package Description30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-919-21) > 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-919-11)
Product NDC68084-919
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFinasteride
Non-Proprietary NameFinasteride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20160407
End Marketing Date20170930
Marketing Category NameANDA
Application NumberANDA090060
ManufacturerAmerican Health Packaging
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/68084-919-21





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