"70518-0021-0" National Drug Code (NDC)

Ondansetron 12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0021-0)
(REMEDYREPACK INC.)

NDC Code70518-0021-0
Package Description12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0021-0)
Product NDC70518-0021
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOndansetron
Non-Proprietary NameOndansetron
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20161129
Marketing Category NameANDA
Application NumberANDA077851
ManufacturerREMEDYREPACK INC.
Substance NameONDANSETRON HYDROCHLORIDE
Strength4
Strength Unitmg/1
Pharmacy ClassesSerotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]

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