Active ingredient
Almotriptan
6 finished FDA listings contain Almotriptan as their only active ingredient.
FDA NDC Directory
- Ingredient names as written by FDA
- ALMOTRIPTAN MALATE
- Dosage forms
- Tablet, Film Coated
- Routes
- Oral
- Manufacturers / labelers
- 3
- Strengths listed
- 12.5 mg/1 · 6.25 mg/1
- Brand names in FDA listings
- Almotriptan Malate
RxNorm (National Library of Medicine)
Ingredient concept RxCUI 279645
Drugs@FDA applications
Linked only where the FDA listing’s application number matches Drugs@FDA exactly. A listing in the NDC Directory does not by itself mean FDA approval.
| Application | Sponsor | Original approval | Listings |
|---|---|---|---|
| ANDA 078027 | TEVA PHARMS USA | 2015-07-07 | 2 |
| ANDA 205171 | MYLAN | 2015-11-09 | 2 |
| ANDA 205523 | AJANTA PHARMA LTD | 2016-03-03 | 2 |
Official labeling on DailyMed
- ALMOTRIPTAN TABLET, FILM COATED [AJANTA PHARMA USA INC.] · version 10 · 2026-01-08
- ALMOTRIPTAN MALATE TABLET, FILM COATED [TEVA PHARMACEUTICALS USA, INC.] · version 6 · 2020-08-28
- ALMOTRIPTAN MALATE (ALMOTRIPTAN) TABLET, FILM COATED [MYLAN PHARMACEUTICALS INC.] · version 4 · 2018-09-26
Sources: FDA NDC Directory (2026-09-29), RxNorm, Drugs@FDA, DailyMed. Each source’s facts are shown separately as published.