FDA NDC Directory · JSON-LD · Markdown

Ondansetron

NDC 68788-7644 · HUMAN PRESCRIPTION DRUG · TABLET, ORALLY DISINTEGRATING

Labeler / ManufacturerPreferred Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090469
Dosage form / routeTABLET, ORALLY DISINTEGRATING · ORAL
Active ingredientsONDANSETRON (4 mg/1)
Marketing started20200228
Package count3

External sources

Source: openFDA. Public-domain (CC0).