FDA NDC Directory · JSON-LD · Markdown

Mexiletine Hydrochloride

NDC 62559-822 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerANI Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA074450
Dosage form / routeCAPSULE · ORAL
Active ingredientsMEXILETINE HYDROCHLORIDE (250 mg/1)
Marketing started20200622
Package count1

External sources

Source: openFDA. Public-domain (CC0).