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"43598-303-30" National Drug Code (NDC)

Finasteride 30 TABLET, FILM COATED in 1 BOTTLE (43598-303-30)
(Dr Reddys Laboratories Inc)

NDC Code43598-303-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE (43598-303-30)
Product NDC43598-303
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFinasteride
Non-Proprietary NameFinasteride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20121025
Marketing Category NameANDA
Application NumberANDA090061
ManufacturerDr Reddys Laboratories 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/43598-303-30





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