Chlorzoxazone
- Product NDC
- 49999-044
- 11-digit product format
- 499990044
- Labeler code
- 49999
- Product ID
- 49999-044_f1a327d4-6fa7-4413-87d9-851a17f441fa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorzoxazone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA089859
- Marketing category
- ANDA
- Marketing start
- 2011-04-12
- Marketing end
- 0000-00-00
- Substance
- CHLORZOXAZONE
- Active strength
- 500 mg/1
- Pharmacologic classes
- Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [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 |
|---|
| 49999-044-30 | 49999004430 | 30 TABLET in 1 BOTTLE, PLASTIC (49999-044-30) | 30 tablet | 2011-04-12 | 0000-00-00 | No | No | Current |
| 49999-044-60 | 49999004460 | 60 TABLET in 1 BOTTLE, PLASTIC (49999-044-60) | 60 tablet | 2011-04-12 | 0000-00-00 | No | No | Current |
| 49999-044-90 | 49999004490 | 90 TABLET in 1 BOTTLE, PLASTIC (49999-044-90) | 90 tablet | 2011-04-12 | 0000-00-00 | No | No | Current |