FDA NDC Directory · JSON-LD · Markdown

Ondansetron Hydrochloride

NDC 68999-555 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerChartwell Governmental & Specialty RX, LLC.
Marketing categoryAbbreviated NDA (generic) · App ANDA091342
Dosage form / routeSOLUTION · ORAL
Active ingredientsONDANSETRON HYDROCHLORIDE (4 mg/5mL)
Marketing started20110127
Package count1

External sources

Source: openFDA. Public-domain (CC0).