FDA NDC Directory · JSON-LD · Markdown

Zolmitriptan

NDC 62332-463 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAlembic Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA204232
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsZOLMITRIPTAN (5 mg/1)
Marketing started20240110
Package count1

External sources

Source: openFDA. Public-domain (CC0).