NDC 63629-2145 – Mexiletine Hydrochloride

Mexiletine Hydrochloride 150 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC63629-2145

Product details

Brand name
Mexiletine Hydrochloride
Generic name
Mexiletine Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA074450
Marketed since
June 22, 2020
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
63629-2145-1100 CAPSULE in 1 BOTTLE (63629-2145-1)Feb 8, 2021

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