# Zolmitriptan

NDC: 68462-497
Generic name: Zolmitriptan
Labeler / Manufacturer: Glenmark Pharmaceuticals Inc.,USA
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20130514

FDA application: ANDA201779

## 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:"68462-497"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68462-497
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=333caafc-2e63-49f8-a0c6-534e528d228d