Active ingredient
Mefloquine
3 finished FDA listings contain Mefloquine as their only active ingredient.
FDA NDC Directory
- Ingredient names as written by FDA
- MEFLOQUINE HYDROCHLORIDE
- Dosage forms
- Tablet
- Routes
- Oral
- Manufacturers / labelers
- 3
- Strengths listed
- 250 mg/1
RxNorm (National Library of Medicine)
Ingredient concept RxCUI 6694
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 076175 | CHARTWELL RX | 2002-02-20 | 1 |
| ANDA 076392 | BARR | 2003-12-29 | 2 |
Official labeling on DailyMed
- MEFLOQUINE HYDROCHLORIDE TABLET [TEVA PHARMACEUTICALS USA, INC.] · version 13 · 2026-02-04
- MEFLOQUINE HYDROCHLORIDE TABLET [A-S MEDICATION SOLUTIONS] · version 12 · 2025-04-07
- MEFLOQUINE HYDROCHLORIDE TABLET [CHARTWELL RX, LLC] · version 1 · 2024-11-20
Sources: FDA NDC Directory (2026-09-29), RxNorm, Drugs@FDA, DailyMed. Each source’s facts are shown separately as published.