Mexiletine Hydrochloride 00093-8741-01

Package NDC

00093-8741-01

Manufacturer: Teva Pharmaceuticals Usa, Inc.
Dosage Form: Capsule
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: June 5, 1995
Listing Expires: December 31, 2026
Application: ANDA074377

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Active Ingredients

Ingredient	Strength
Mexiletine Hydrochloride	250 mg/1

Drug Class

Antiarrhythmic [EPC]

Selected Package

00093-8741-01Selected

100 CAPSULE in 1 BOTTLE (0093-8741-01)