"0781-1679-31" National Drug Code (NDC)

Ondansetron 30 TABLET, FILM COATED in 1 BOTTLE (0781-1679-31)
(Sandoz Inc)

NDC Code0781-1679-31
Package Description30 TABLET, FILM COATED in 1 BOTTLE (0781-1679-31)
Product NDC0781-1679
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOndansetron
Non-Proprietary NameOndansetron
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20070625
End Marketing Date20191130
Marketing Category NameANDA
Application NumberANDA077517
ManufacturerSandoz Inc
Substance NameONDANSETRON HYDROCHLORIDE
Strength4
Strength Unitmg/1
Pharmacy ClassesSerotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]

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