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MEXILETINE HYDROCHLORIDE

NDC 50742-239 · HUMAN PRESCRIPTION DRUG · CAPSULE

Generic nameMexiletine hydrochloride
Labeler / ManufacturerIngenus Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA214352
Dosage form / routeCAPSULE · ORAL
Active ingredientsMEXILETINE HYDROCHLORIDE (150 mg/1)
Marketing started20210126
Package count1

External sources

Source: openFDA. Public-domain (CC0).