# Topiramate

NDC: 68462-110
Generic name: Topiramate
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: 20090327

FDA application: ANDA077627

## Active ingredients

- TOPIRAMATE: 200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68462-110"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68462-110
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=35312f49-decf-428d-bf5f-4215b762ed3c