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"0093-7355-05" National Drug Code (NDC)

Finasteride 500 TABLET, FILM COATED in 1 BOTTLE (0093-7355-05)
(Teva Pharmaceuticals USA, Inc.)

NDC Code0093-7355-05
Package Description500 TABLET, FILM COATED in 1 BOTTLE (0093-7355-05)
Product NDC0093-7355
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFinasteride
Non-Proprietary NameFinasteride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20061215
End Marketing Date20260930
Marketing Category NameANDA
Application NumberANDA076511
ManufacturerTeva 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/0093-7355-05





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