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MEXILETINE HYDROCHLORIDE

NDC 82012-027 · HUMAN PRESCRIPTION DRUG · CAPSULE

Generic namemexiletine hydrochloride
Labeler / ManufacturerSenores Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA202111
Dosage form / routeCAPSULE · ORAL
Active ingredientsMEXILETINE HYDROCHLORIDE (150 mg/1)
Marketing started20200307
Package count1

External sources

Source: openFDA. Public-domain (CC0).