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"71335-0132-2" National Drug Code (NDC)

Ondansetron 3 TABLET, FILM COATED in 1 BOTTLE (71335-0132-2)
(Bryant Ranch Prepack)

NDC Code71335-0132-2
Package Description3 TABLET, FILM COATED in 1 BOTTLE (71335-0132-2)
Product NDC71335-0132
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOndansetron
Non-Proprietary NameOndansetron
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20070727
Marketing Category NameANDA
Application NumberANDA077851
ManufacturerBryant Ranch Prepack
Substance NameONDANSETRON HYDROCHLORIDE
Strength4
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/71335-0132-2





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