Tizanidine Hydrochloride
- Product NDC
- 55700-789
- 11-digit product format
- 557000789
- Labeler code
- 55700
- Product ID
- 55700-789_d77fc799-f96f-4376-bc8d-d1f42e60e536
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tizanidine Hydrochloride
- Dosage form
- CAPSULE, GELATIN COATED
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA078868
- Marketing category
- ANDA
- Marketing start
- 2019-09-06
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-789-30 | 55700078930 | 30 CAPSULE, GELATIN COATED in 1 BOTTLE (55700-789-30) | 2019-09-06 | 0000-00-00 | No | No | Current |