FDA NDC

Mexiletine Hydrochloride

This name is from the loaded FDA file.

Source: FDA NDC Directory, live from openFDA. Publisher page

NDC
62559-821
Proprietary name
Mexiletine Hydrochloride
Nonproprietary name
Mexiletine Hydrochloride
Labeler
ANI Pharmaceuticals, Inc.
Dosage form
CAPSULE
Strength
200 mg/1

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