Mexiletine Hydrochloride 62559-0821-01

Package NDC

62559-0821-01

Manufacturer: Ani Pharmaceuticals, Inc.
Dosage Form: Capsule
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: June 22, 2020
Listing Expires: December 31, 2026
Application: ANDA074450

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Active Ingredients

Ingredient	Strength
Mexiletine Hydrochloride	200 mg/1

Drug Class

Antiarrhythmic [EPC]

Selected Package

62559-0821-01Selected

100 CAPSULE in 1 BOTTLE (62559-821-01)