Tizanidine
- Product NDC
- 60760-782
- 11-digit product format
- 607600782
- Labeler code
- 60760
- Product ID
- 60760-782_d27edbe7-6063-e0aa-e053-2a95a90a0cf2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tizanidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA091283
- Marketing category
- ANDA
- Marketing start
- 2000-08-18
- Marketing end
- 0000-00-00
- Substance
- TIZANIDINE HYDROCHLORIDE
- Active strength
- 2 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-782-04 | 60760078204 | 4 TABLET in 1 BOTTLE, PLASTIC (60760-782-04) | 4 tablet | 2020-03-30 | 0000-00-00 | No | No | Current |
| 60760-782-15 | 60760078215 | 15 TABLET in 1 BOTTLE, PLASTIC (60760-782-15) | 15 tablet | 2018-10-11 | 0000-00-00 | No | No | Current |
| 60760-782-30 | 60760078230 | 30 TABLET in 1 BOTTLE, PLASTIC (60760-782-30) | 30 tablet | 2015-08-18 | 0000-00-00 | No | No | Current |
| 60760-782-90 | 60760078290 | 90 TABLET in 1 BOTTLE, PLASTIC (60760-782-90) | 90 tablet | 2015-08-18 | 0000-00-00 | No | No | Current |