FDA NDC Directory · JSON-LD · Markdown

Mexiletine Hydrochloride

NDC 42291-625 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerAvKARE
Marketing categoryAbbreviated NDA (generic) · App ANDA074377
Dosage form / routeCAPSULE · ORAL
Active ingredientsMEXILETINE HYDROCHLORIDE (200 mg/1)
Marketing started20130709
Package count1

External sources

Source: openFDA. Public-domain (CC0).