Mexiletine Hydrochloride 33342-0557
Product NDC
33342-0557- Manufacturer
- Macleods Pharmaceuticals Limited
- Dosage Form
- Capsule
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 23, 2026
- Listing Expires
- December 31, 2027
- Application
- ANDA219987
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Mexiletine Hydrochloride | 200 mg/1 |
Drug Class
Antiarrhythmic [EPC]
Packaging Options(2)
100 CAPSULE in 1 CONTAINER (33342-557-11)
10 BLISTER PACK in 1 CARTON (33342-557-12) / 10 CAPSULE in 1 BLISTER PACK