United States · FDA National Drug Code directory
Eletriptan Hydrobromide
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 0378-4287_cba8e2c4-eb4b-49c7-83be-d5cfb58b23d9
- Product NDC
- 0378-4287
- Form
- TABLET, FILM COATED
- Composition / generic term
- eletriptan hydrobromide
- Labeler
- Mylan Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170815
- Source listing expiry
- 20261231
Source-listed ingredients
- ELETRIPTAN HYDROBROMIDE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BLISTER PACK in 1 CARTON (0378-4287-85) / 6 TABLET, FILM COATED in 1 BLISTER PACK (0378-4287-32) · 0378-4287-85
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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