Tizanidine
- Product NDC
- 72189-602
- 11-digit product format
- 721890602
- Labeler code
- 72189
- Product ID
- 72189-602_2d4108dc-4f74-69fb-e063-6294a90a10f8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tizanidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct_rx
- Application
- ANDA076416
- Marketing category
- ANDA
- Marketing start
- 2024-12-31
- Substance
- TIZANIDINE HYDROCHLORIDE
- Active strength
- 4 mg/1
- Pharmacologic classes
- Adrenergic alpha2-Agonists [MoA], Central alpha-2 Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| B53E3NMY5C | TIZANIDINE HYDROCHLORIDE | 64461-82-1 | TIZANIDINE HYDROCHLORIDE |
| 6AI06C00GW | TIZANIDINE | 51322-75-9 | Tizanidine |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72189-602-30 | 72189060230 | 30 TABLET in 1 BOTTLE (72189-602-30) | 30 tablet | 2024-12-31 | No | No | Historical |
| 72189-602-60 | 72189060260 | 60 TABLET in 1 BOTTLE (72189-602-60) | 60 tablet | 2024-12-31 | No | No | Historical |
| 72189-602-90 | 72189060290 | 90 TABLET in 1 BOTTLE (72189-602-90) | 90 tablet | 2024-12-31 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Tizanidine | Direct_rx | 2025-02-03 | HUMAN PRESCRIPTION DRUG LABEL | 3 |