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Zolmitriptan

NDC 63548-0102 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerPLD Acquisitions LLC DBA Avma Pharma Solutions
Marketing categoryAbbreviated NDA (generic) · App ANDA207867
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsZOLMITRIPTAN (5 mg/1)
Marketing started20170227
Package count1

External sources

Source: openFDA. Public-domain (CC0).