NDC 60687-778 – Mexiletine hydrochloride

Mexiletine Hydrochloride 150 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC60687-778

Product details

Brand name
Mexiletine hydrochloride
Generic name
Mexiletine hydrochloride
Labeler
American Health Packaging
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA216463
Marketed since
February 23, 2024
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
60687-778-2130 BLISTER PACK in 1 CARTON (60687-778-21) / 1 CAPSULE in 1 BLISTER PACK (60687-778-11)Feb 23, 2024

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