chlorzoxazone
- Product NDC
- 46672-118
- 11-digit product format
- 466720118
- Labeler code
- 46672
- Product ID
- 46672-118_9c56a823-bf66-3005-e053-2a95a90a22e3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- chlorzoxazone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Mikart, LLC
- Application
- ANDA040861
- Marketing category
- ANDA
- Marketing start
- 2010-06-01
- Marketing end
- 0000-00-00
- Substance
- CHLORZOXAZONE
- Active strength
- 375 mg/1
- Pharmacologic classes
- Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 46672-118-10 | 46672011810 | 100 TABLET in 1 BOTTLE (46672-118-10) | 100 tablet | 2010-06-01 | 0000-00-00 | No | No | Current |
| 46672-118-50 | 46672011850 | 500 TABLET in 1 BOTTLE (46672-118-50) | 500 tablet | 2010-06-01 | 0000-00-00 | No | No | Current |