NDC 33342-556 – Mexiletine Hydrochloride
Mexiletine Hydrochloride 200 mg/1 · Capsule · Oral
Product NDC33342-556
Product details
- Brand name
- Mexiletine Hydrochloride
- Generic name
- Mexiletine Hydrochloride
- Labeler
- Macleods Pharmaceuticals Limited
- Dosage form
- Capsule
- Route
- Oral
- Marketing category
- ANDA · ANDA219987
- Marketed since
- March 23, 2026
- Listing expires
- December 31, 2027
- Pharmacologic class
- Antiarrhythmic
Active ingredients
- Mexiletine Hydrochloride 200 mg/1
Uses, dosage, side effects and warnings for Mexiletine Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 33342-556-11 | 100 CAPSULE in 1 CONTAINER (33342-556-11) | Mar 23, 2026 |
| 33342-556-12 | 10 BLISTER PACK in 1 CARTON (33342-556-12) / 10 CAPSULE in 1 BLISTER PACK | Mar 23, 2026 |
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