Tizanidine Hydrochloride
- Product NDC
- 71335-0317
- 11-digit product format
- 713350317
- Labeler code
- 71335
- Product ID
- 71335-0317_93de2f10-747a-4518-85aa-de93552e1194
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tizanidine Hydrochloride
- Dosage form
- CAPSULE, GELATIN COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078868
- Marketing category
- ANDA
- Marketing start
- 2012-02-06
- Marketing end
- 0000-00-00
- Substance
- TIZANIDINE HYDROCHLORIDE
- Active strength
- 6 mg/1
- Pharmacologic classes
- Adrenergic alpha2-Agonists [MoA], Central alpha-2 Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0317-1 | 71335031701 | 30 CAPSULE, GELATIN COATED in 1 BOTTLE (71335-0317-1) | 2015-04-24 | 0000-00-00 | No | No | Current |
| 71335-0317-2 | 71335031702 | 60 CAPSULE, GELATIN COATED in 1 BOTTLE (71335-0317-2) | 2015-04-24 | 0000-00-00 | No | No | Current |
| 71335-0317-3 | 71335031703 | 90 CAPSULE, GELATIN COATED in 1 BOTTLE (71335-0317-3) | 2015-04-24 | 0000-00-00 | No | No | Current |
| 71335-0317-4 | 71335031704 | 120 CAPSULE, GELATIN COATED in 1 BOTTLE (71335-0317-4) | 2015-04-24 | 0000-00-00 | No | No | Current |
| 71335-0317-5 | 71335031705 | 28 CAPSULE, GELATIN COATED in 1 BOTTLE (71335-0317-5) | 2015-04-24 | 0000-00-00 | No | No | Current |