United States · FDA National Drug Code directory
Mefloquine Hydrochloride
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
- 62135-973_2732839a-191a-570f-e063-6294a90a40a4
- Product NDC
- 62135-973
- Form
- TABLET
- Composition / generic term
- Mefloquine Hydrochloride
- Labeler
- Chartwell RX, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220220
- Source listing expiry
- 20261231
Source-listed ingredients
- MEFLOQUINE HYDROCHLORIDE — 250 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 5 TABLET in 1 BOTTLE (62135-973-11) · 62135-973-11
- 25 TABLET in 1 BOTTLE (62135-973-25) · 62135-973-25
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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