Mexiletine Hydrochloride 82012-0027
Product NDC
82012-0027- Manufacturer
- Senores Pharmaceuticals, Inc.
- Dosage Form
- Capsule
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 7, 2020
- Listing Expires
- December 31, 2026
- Application
- ANDA202111
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Mexiletine Hydrochloride | 150 mg/1 |
Drug Class
Antiarrhythmic [EPC]
Packaging Options(1)
100 CAPSULE in 1 BOTTLE (82012-027-04)