FDA NDC Directory · JSON-LD · Markdown

Zonisamide

NDC 68462-129 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerGlenmark Pharmaceuticals Inc., USA
Marketing categoryAbbreviated NDA (generic) · App ANDA077651
Dosage form / routeCAPSULE · ORAL
Active ingredientsZONISAMIDE (50 mg/1)
Marketing started20060130
Package count2

External sources

Source: openFDA. Public-domain (CC0).