← FDA Drug Approvals (Drugs@FDA)
MEXILETINE HYDROCHLORIDE
ANDA · Abbreviated New Drug Application (Generic) · Sponsor: WATSON LABS · Approved 1998-04-13
Drug application
- FDA Application #
ANDA074865- 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
- Discontinued
- Sponsor
- WATSON LABS
- First approval
- 1998-04-13
Source
- Authoritative
- Drugs@FDA application overview
- Machine
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