Mexiletine Hydrochloride 50742-0240
Product NDC
50742-0240- Manufacturer
- Ingenus Pharmaceuticals, Llc
- Dosage Form
- Capsule
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 26, 2021
- Listing Expires
- December 31, 2026
- Application
- ANDA214352
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Mexiletine Hydrochloride | 200 mg/1 |
Drug Class
Antiarrhythmic [EPC]
Packaging Options(1)
100 CAPSULE in 1 BOTTLE (50742-240-01)