United States · FDA National Drug Code directory
Almotriptan Malate
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
- 0093-5261_3c9afddb-516b-43a3-9a28-9a3b3aca6340
- Product NDC
- 0093-5261
- Form
- TABLET, FILM COATED
- Composition / generic term
- Almotriptan Malate
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20150707
- Source listing expiry
- 20261231
Source-listed ingredients
- ALMOTRIPTAN MALATE — 12.5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 12 BLISTER PACK in 1 CARTON (0093-5261-29) / 1 TABLET, FILM COATED in 1 BLISTER PACK (0093-5261-19) · 0093-5261-29
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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