NDC 31722-036 – Mexiletine hydrochloride

Mexiletine Hydrochloride 150 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC31722-036

Product details

Brand name
Mexiletine hydrochloride
Generic name
Mexiletine hydrochloride
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA216463
Marketed since
November 9, 2022
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
31722-036-01100 CAPSULE in 1 BOTTLE (31722-036-01)Nov 9, 2022

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