NDC 62559-820 – Mexiletine Hydrochloride

Mexiletine Hydrochloride 150 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC62559-820

Product details

Brand name
Mexiletine Hydrochloride
Generic name
Mexiletine Hydrochloride
Labeler
ANI Pharmaceuticals, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA074450
Marketed since
June 22, 2020
Listing expires
December 31, 2026
Pharmacologic class
Antiarrhythmic

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
62559-820-01100 CAPSULE in 1 BOTTLE (62559-820-01)Jun 22, 2020

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