FDA NDC Directory · JSON-LD · Markdown

MEXILETINE HYDROCHLORIDE

NDC 87564-054 · HUMAN PRESCRIPTION DRUG · CAPSULE

Generic namemexiletine hydrochloride
Labeler / ManufacturerAmerisyn LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA214089
Dosage form / routeCAPSULE · ORAL
Active ingredientsMEXILETINE HYDROCHLORIDE (250 mg/1)
Marketing started20260806
Package count1

External sources

Source: openFDA. Public-domain (CC0).