# MEXILETINE HYDROCHLORIDE
> **ANDA074377** · Abbreviated New Drug Application (Generic) · Sponsor: TEVA · Approved 1995-05-16
## Drug
- **FDA Application Number:** ANDA074377
- **Application type:** Abbreviated New Drug Application (Generic)
- **Brand name:** MEXILETINE HYDROCHLORIDE
- **Generic name:** MEXILETINE HYDROCHLORIDE
- **Active ingredients:** MEXILETINE HYDROCHLORIDE
- **Dosage form:** CAPSULE
- **Route:** ORAL
- **Marketing status:** Prescription
- **Sponsor:** TEVA
- **Manufacturer:** Teva Pharmaceuticals USA, Inc.
- **First approval:** 1995-05-16
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=074377)
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