FDA NDC Directory · JSON-LD · Markdown

MEXILETINE HYDROCHLORIDE

NDC 63629-9181 · HUMAN PRESCRIPTION DRUG · CAPSULE

Generic namemexiletine hydrochloride
Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA214089
Dosage form / routeCAPSULE · ORAL
Active ingredientsMEXILETINE HYDROCHLORIDE (250 mg/1)
Marketing started20211129
Package count1

External sources

Source: openFDA. Public-domain (CC0).