United States · FDA National Drug Code directory
almotriptan
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
- 27241-042_caa5857a-45bf-4b7d-8874-6fe2cb6eb4cf
- Product NDC
- 27241-042
- Form
- TABLET, FILM COATED
- Composition / generic term
- almotriptan
- Labeler
- Ajanta Pharma USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20151007
- Source listing expiry
- 20271231
Source-listed ingredients
- ALMOTRIPTAN MALATE — 12.5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 2 BLISTER PACK in 1 CARTON (27241-042-21) / 6 TABLET, FILM COATED in 1 BLISTER PACK (27241-042-68) · 27241-042-21
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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