NDC 63629-9180 – Mexiletine Hydrochloride

Mexiletine Hydrochloride 200 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC63629-9180

Product details

Brand name
Mexiletine Hydrochloride
Generic name
Mexiletine hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA214089
Marketed since
November 29, 2021
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
63629-9180-1100 CAPSULE in 1 BOTTLE (63629-9180-1)Feb 22, 2022

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