"42291-280-30" National Drug Code (NDC)

Finasteride 30 TABLET, FILM COATED in 1 BOTTLE (42291-280-30)
(AvKARE, Inc.)

NDC Code42291-280-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE (42291-280-30)
Product NDC42291-280
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFinasteride
Non-Proprietary NameFinasteride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20130226
Marketing Category NameANDA
Application NumberANDA076511
ManufacturerAvKARE, Inc.
Substance NameFINASTERIDE
Strength5
Strength Unitmg/1
Pharmacy Classes5-alpha Reductase Inhibitor [EPC],5-alpha Reductase Inhibitors [MoA]

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