Mexiletine Hydrochloride 00527-4108-37

Package NDC

00527-4108-37

Manufacturer: Lannett Company, Inc.
Dosage Form: Capsule
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: July 23, 2020
Listing Expires: December 31, 2026
Application: ANDA213500

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Active Ingredients

Ingredient	Strength
Mexiletine Hydrochloride	200 mg/1

Drug Class

Antiarrhythmic [EPC]

Selected Package

00527-4108-37Selected

100 CAPSULE in 1 BOTTLE (0527-4108-37)