# Mexiletine Hydrochloride

NDC: 63629-1963
Generic name: Mexiletine Hydrochloride
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20200622

FDA application: ANDA074450

## Active ingredients

- MEXILETINE HYDROCHLORIDE: 200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63629-1963"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63629-1963
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b1cb1e35-9586-41c4-b43f-c517f2d42f31