"70934-193-06" National Drug Code (NDC)

Ondansetron Hydrochloride 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-193-06)
(Denton Pharma, Inc. DBA Northwind Pharmaceuticals)

NDC Code70934-193-06
Package Description6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-193-06)
Product NDC70934-193
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOndansetron Hydrochloride
Non-Proprietary NameOndansetron Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20181112
End Marketing Date20231231
Marketing Category NameANDA
Application NumberANDA078539
ManufacturerDenton Pharma, Inc. DBA Northwind Pharmaceuticals
Substance NameONDANSETRON HYDROCHLORIDE
Strength8
Strength Unitmg/1
Pharmacy ClassesSerotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC]

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