# Zolmitriptan

NDC: 65841-767
Generic name: Zolmitriptan
Labeler / Manufacturer: Zydus Lifesciences Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, ORALLY DISINTEGRATING
Routes: ORAL
Marketing started: 20130516

FDA application: ANDA202890

## 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:"65841-767"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65841-767
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=aae2d9cb-9938-4032-961f-f0afd1958b5d