Mexiletine Hydrochloride 64980-0667-01

Package NDC

64980-0667-01

Manufacturer: Rising Pharma Holdings, Inc.
Dosage Form: Capsule
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: February 5, 2025
Listing Expires: December 31, 2026
Application: ANDA215315

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Active Ingredients

Ingredient	Strength
Mexiletine Hydrochloride	200 mg/1

Drug Class

Antiarrhythmic [EPC]

Selected Package

64980-0667-01Selected

100 CAPSULE in 1 BOTTLE (64980-667-01)