NDC 62756-956 – Mexiletine Hydrochloride
Mexiletine Hydrochloride 200 mg/1 · Capsule · Oral
Product NDC62756-956
Product details
- Brand name
- Mexiletine Hydrochloride
- Generic name
- Mexiletine hydrochloride
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Capsule
- Route
- Oral
- Marketing category
- ANDA · ANDA214089
- Marketed since
- November 29, 2021
- Listing expires
- December 31, 2026
- Pharmacologic class
- Antiarrhythmic
Active ingredients
- Mexiletine Hydrochloride 200 mg/1
Uses, dosage, side effects and warnings for Mexiletine Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 62756-956-01 | 100 CAPSULE in 1 BOTTLE (62756-956-01) | Nov 29, 2021 |
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