Tizanidine
- Product NDC
- 72189-526
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tizanidine
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA210267
- Marketing category
- ANDA
- Substance
- TIZANIDINE HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 72189-526-30 | 30 CAPSULE in 1 BOTTLE (72189-526-30) | 2023-12-06 | | No | Historical |
| 72189-526-60 | 60 CAPSULE in 1 BOTTLE (72189-526-60) | 2023-12-06 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Tizanidine | Direct_Rx | 2025-08-19 | HUMAN PRESCRIPTION DRUG LABEL | 4 |