www.ndcvalidator.com
National Drug Code Lookup | NDC Directory | About | Feedback

"47335-715-81" National Drug Code (NDC)

Finasteride 90 TABLET, FILM COATED in 1 BOTTLE (47335-715-81)
(Sun Pharmaceutical Industries, Inc.)

NDC Code47335-715-81
Package Description90 TABLET, FILM COATED in 1 BOTTLE (47335-715-81)
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/47335-715-81





Copyright © 2007-2024 www.ndcvalidator.com