# Eletriptan Hydrobromide

NDC: 0378-4288
Generic name: eletriptan hydrobromide
Labeler / Manufacturer: Mylan Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20170815

FDA application: ANDA205152

## Active ingredients

- ELETRIPTAN HYDROBROMIDE: 40 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0378-4288"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0378-4288
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=20276f5c-f2d6-469f-9a1b-aa254a1db21c