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Ondansetron

NDC 70518-3512 · HUMAN PRESCRIPTION DRUG · TABLET, ORALLY DISINTEGRATING

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA078152
Dosage form / routeTABLET, ORALLY DISINTEGRATING · ORAL
Active ingredientsONDANSETRON (4 mg/1)
Marketing started20220907
Package count6

External sources

Source: openFDA. Public-domain (CC0).