"70518-1585-4" National Drug Code (NDC)

Ondansetron Hydrochloride 16 TABLET, FILM COATED in 1 BLISTER PACK (70518-1585-4)
(REMEDYREPACK INC.)

NDC Code70518-1585-4
Package Description16 TABLET, FILM COATED in 1 BLISTER PACK (70518-1585-4)
Product NDC70518-1585
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOndansetron Hydrochloride
Non-Proprietary NameOndansetron Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20181024
Marketing Category NameANDA
Application NumberANDA078539
ManufacturerREMEDYREPACK INC.
Substance NameONDANSETRON HYDROCHLORIDE
Strength4
Strength Unitmg/1
Pharmacy ClassesSerotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC]

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