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
- 70771-1108_b0459347-b3de-466e-b386-85665dd294c9
- Product NDC
- 70771-1108
- Form
- TABLET, FILM COATED
- Composition / generic term
- Eletriptan hydrobromide
- Labeler
- Zydus Lifesciences Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170712
- Source listing expiry
- 20261231
Source-listed ingredients
- ELETRIPTAN HYDROBROMIDE — 40 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE (70771-1108-3) · 70771-1108-3
- 10 BLISTER PACK in 1 CARTON (70771-1108-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1108-2) · 70771-1108-4
- 500 TABLET, FILM COATED in 1 BOTTLE (70771-1108-5) · 70771-1108-5
- 1 BLISTER PACK in 1 CARTON (70771-1108-6) / 6 TABLET, FILM COATED in 1 BLISTER PACK · 70771-1108-6
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →