Tizanidine
- Product NDC
- 0904-6898
- 11-digit product format
- 009046898
- Labeler code
- 0904
- Product ID
- 0904-6898_dbf630d1-94f5-4d3c-bf99-3bbb09f7e649
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tizanidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA076416
- Marketing category
- ANDA
- Marketing start
- 2003-12-11
- Marketing end
- 0000-00-00
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0904-6898-92 | 00904689892 | 150 TABLET in 1 BOTTLE (0904-6898-92) | 150 tablet | 2003-12-11 | 0000-00-00 | No | No | Current |