# eletriptan hydrobromide

NDC: 55700-756
Generic name: eletriptan hydrobromide
Labeler / Manufacturer: Quality Care Products, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20190524
Marketing ended: 20260630
FDA application: ANDA205186

## 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:"55700-756"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55700-756
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1728c511-d1fd-4e30-85ba-f0f5d996088b