United States · FDA National Drug Code directory

Relpax

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
58151-367_ca50a848-b287-47b6-980b-5729d4582893
Product NDC
58151-367
Form
TABLET
Composition / generic term
eletriptan hydrobromide
Labeler
Viatris Specialty LLC
Marketing category
NDA
Marketing start / end (source format)
20250508
Source listing expiry
20261231

Source-listed ingredients

  • ELETRIPTAN HYDROBROMIDE — 20 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 6 BLISTER PACK in 1 CARTON (58151-367-56) / 1 TABLET in 1 BLISTER PACK · 58151-367-56

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.

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