United States · FDA National Drug Code directory
Mexiletine 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
- 33342-556_ee39f605-54ac-4537-a1cb-e3dd33c62ab2
- Product NDC
- 33342-556
- Form
- CAPSULE
- Composition / generic term
- Mexiletine Hydrochloride
- Labeler
- Macleods Pharmaceuticals Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260323
- Source listing expiry
- 20271231
Source-listed ingredients
- MEXILETINE HYDROCHLORIDE — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 CAPSULE in 1 CONTAINER (33342-556-11) · 33342-556-11
- 10 BLISTER PACK in 1 CARTON (33342-556-12) / 10 CAPSULE in 1 BLISTER PACK · 33342-556-12
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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