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"47335-715-13" National Drug Code (NDC)

Finasteride 500 TABLET, FILM COATED in 1 BOTTLE (47335-715-13)
(Sun Pharmaceutical Industries, Inc.)

NDC Code47335-715-13
Package Description500 TABLET, FILM COATED in 1 BOTTLE (47335-715-13)
Product NDC47335-715
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFinasteride
Non-Proprietary NameFinasteride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20221125
Marketing Category NameANDA
Application NumberANDA090507
ManufacturerSun Pharmaceutical Industries, 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/47335-715-13





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