"82009-061-05" National Drug Code (NDC)

Finasteride 500 TABLET, FILM COATED in 1 BOTTLE (82009-061-05)
(QUALLENT PHARMACEUTICALS HEALTH LLC)

NDC Code82009-061-05
Package Description500 TABLET, FILM COATED in 1 BOTTLE (82009-061-05)
Product NDC82009-061
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFinasteride
Non-Proprietary NameFinasteride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20221121
Marketing Category NameANDA
Application NumberANDA078341
ManufacturerQUALLENT PHARMACEUTICALS HEALTH LLC
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/82009-061-05