# Zolmitriptan

NDC: 65862-914
Generic name: Zolmitriptan
Labeler / Manufacturer: Aurobindo Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20160511

FDA application: ANDA207021

## Active ingredients

- ZOLMITRIPTAN: 2.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65862-914"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65862-914
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9212b076-b1ae-4c06-bd56-0ae3c5c9acdf