FDA NDC Directory · JSON-LD · Markdown

Zarontin

NDC 0071-2418 · HUMAN PRESCRIPTION DRUG · SOLUTION

Generic nameEthosuximide
Labeler / ManufacturerParke-Davis Div of Pfizer Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA080258
Dosage form / routeSOLUTION · ORAL
Active ingredientsETHOSUXIMIDE (250 mg/5mL)
Marketing started20200310
Package count1

External sources

Source: openFDA. Public-domain (CC0).