# Sumatriptan Succinate

NDC: 0378-5632
Generic name: sumatriptan succinate
Labeler / Manufacturer: Mylan Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20090810

FDA application: ANDA077744

## Active ingredients

- SUMATRIPTAN SUCCINATE: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0378-5632"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0378-5632
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1d2cd01c-05e7-44cf-a71d-0f474e826b7e