FDA NDC Directory · JSON-LD · Markdown

Ondansetron

NDC 17856-0691 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerATLANTIC BIOLOGICALS CORP.
Marketing categoryAbbreviated NDA (generic) · App ANDA091483
Dosage form / routeSOLUTION · ORAL
Active ingredientsONDANSETRON HYDROCHLORIDE (4 mg/5mL)
Marketing started20101217
Package count7

External sources

Source: openFDA. Public-domain (CC0).