NDC 62756-956-01
MEXILETINE HYDROCHLORIDE 200 mg/1
mexiletine hydrochloride · CAPSULE
MEXILETINE HYDROCHLORIDE is a capsule containing mexiletine hydrochloride at a strength of 200 mg/1. Manufactured by Sun Pharmaceutical Industries, Inc..
Key Facts
- Brand Name
- MEXILETINE HYDROCHLORIDE
- Generic Name
- mexiletine hydrochloride
- NDC Code (Package)
62756-956-01- NDC Code (Product)
62756-956- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Strength
- 200 mg/1
- Dosage Form
- CAPSULE
- Route
- ORAL
- Marketing Status
- Application #
- ANDA214089
- Marketing Start
- 11/29/2021
Recall History
No Recall HistoryView Full Drug Page
MEXILETINE HYDROCHLORIDE — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.