"71335-1612-1" National Drug Code (NDC)

Ondansetron Hydrochloride 10 TABLET, FILM COATED in 1 BOTTLE (71335-1612-1)
(Bryant Ranch Prepack)

NDC Code71335-1612-1
Package Description10 TABLET, FILM COATED in 1 BOTTLE (71335-1612-1)
Product NDC71335-1612
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOndansetron Hydrochloride
Non-Proprietary NameOndansetron Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20070731
Marketing Category NameANDA
Application NumberANDA078539
ManufacturerBryant Ranch Prepack
Substance NameONDANSETRON HYDROCHLORIDE
Strength8
Strength Unitmg/1
Pharmacy ClassesSerotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC]

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