FDA NDC Directory · JSON-LD · Markdown

Mexiletine Hydrochloride

NDC 0527-4108 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerLannett Company, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA213500
Dosage form / routeCAPSULE · ORAL
Active ingredientsMEXILETINE HYDROCHLORIDE (200 mg/1)
Marketing started20200723
Package count1

External sources

Source: openFDA. Public-domain (CC0).