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"71335-1612-8" National Drug Code (NDC)

Ondansetron Hydrochloride 60 TABLET, FILM COATED in 1 BOTTLE (71335-1612-8)
(Bryant Ranch Prepack)

NDC Code71335-1612-8
Package Description60 TABLET, FILM COATED in 1 BOTTLE (71335-1612-8)
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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71335-1612-8





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