NDC 87564-053 – Mexiletine Hydrochloride

Mexiletine Hydrochloride 200 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC87564-053

Product details

Brand name
Mexiletine Hydrochloride
Generic name
Mexiletine hydrochloride
Labeler
Amerisyn LLC
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA214089
Marketed since
August 6, 2026
Listing expires
December 31, 2027
Pharmacologic class
Antiarrhythmic

Active ingredients

Uses, dosage, side effects and warnings for Mexiletine Hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
87564-053-10100 CAPSULE in 1 BOTTLE (87564-053-10)Aug 6, 2026

Other Mexiletine Hydrochloride products