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MEXILETINE HYDROCHLORIDE

ANDA · Abbreviated New Drug Application (Generic) · Sponsor: TEVA · Approved 1995-05-16

Drug application

FDA Application #

ANDA074377

Application type

Abbreviated New Drug Application (Generic)

Brand name

MEXILETINE HYDROCHLORIDE

Generic name

MEXILETINE HYDROCHLORIDE

Active ingredients

MEXILETINE HYDROCHLORIDE

Dosage form

CAPSULE

Route

ORAL

Marketing status

Prescription

Sponsor

TEVA

Manufacturer

Teva Pharmaceuticals USA, Inc.

First approval

1995-05-16

Source

Authoritative

Drugs@FDA application overview

Machine

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