Tizanidine
- Product NDC
- 72162-1642
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tizanidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076416
- Marketing category
- ANDA
- Substance
- TIZANIDINE HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 72162-1642-0 | 1000 TABLET in 1 BOTTLE (72162-1642-0) | 2023-10-09 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Tizanidine | Bryant Ranch Prepack | 2023-11-29 | HUMAN PRESCRIPTION DRUG LABEL | 101 |