FDA NDC Directory · JSON-LD · Markdown

Zolmitriptan

NDC 68462-498 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerGlenmark Pharmaceuticals Inc.,USA
Marketing categoryAbbreviated NDA (generic) · App ANDA201779
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsZOLMITRIPTAN (5 mg/1)
Marketing started20130514
Package count1

External sources

Source: openFDA. Public-domain (CC0).