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: 50742-240_64851116-6653-4b86-9bc0-24f93b4ece10
Product NDC: 50742-240
Form: CAPSULE
Composition / generic term: Mexiletine hydrochloride
Labeler: Ingenus Pharmaceuticals, LLC
Marketing category: ANDA
Marketing start / end (source format): 20210126
Source listing expiry: 20261231

Source-listed ingredients

MEXILETINE HYDROCHLORIDE — 200 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

100 CAPSULE in 1 BOTTLE (50742-240-01) · 50742-240-01

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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