← FDA Drug Approvals (Drugs@FDA)
ZANAFLEX
NDA · New Drug Application · Sponsor: LEGACY PHARMA USA · Approved 1996-11-27
Drug application
- FDA Application #
NDA020397- Application type
- New Drug Application
- Brand name
- ZANAFLEX
- Generic name
- TIZANIDINE HYDROCHLORIDE
- Active ingredients
- TIZANIDINE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Marketing status
- Discontinued
- Sponsor
- LEGACY PHARMA USA
- Manufacturer
- Covis Pharma US, Inc
- First approval
- 1996-11-27
Source
- Authoritative
- Drugs@FDA application overview
- Machine
- JSON-LD · Markdown