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"0781-1681-33" National Drug Code (NDC)

Ondansetron 1 BLISTER PACK in 1 CARTON (0781-1681-33) > 3 TABLET, FILM COATED in 1 BLISTER PACK
(Sandoz Inc)

NDC Code0781-1681-33
Package Description1 BLISTER PACK in 1 CARTON (0781-1681-33) > 3 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC0781-1681
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
Strength8
Strength Unitmg/1
Pharmacy ClassesSerotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]

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