# Zolmitriptan

NDC: 63548-0101
Generic name: Zolmitriptan
Labeler / Manufacturer: PLD Acquisitions LLC DBA Avma Pharma Solutions
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20170227

FDA application: ANDA207867

## Active ingredients

- ZOLMITRIPTAN: 2.5 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63548-0101"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63548-0101
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f59bfbdd-7f4b-4a29-8396-e144dde65878