Chlorzoxazone
- Product NDC
- 63629-2000
- 11-digit product format
- 636292000
- Labeler code
- 63629
- Product ID
- 63629-2000_484500b5-98de-4fa5-8634-9d87168d1c3c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorzoxazone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA212254
- Marketing category
- ANDA
- Marketing start
- 2019-11-27
- Marketing end
- 0000-00-00
- Substance
- CHLORZOXAZONE
- Active strength
- 750 mg/1
- Pharmacologic classes
- Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 63629-2000-1 | 63629200001 | 100 TABLET in 1 BOTTLE, PLASTIC (63629-2000-1) | 100 tablet | 2021-07-01 | 0000-00-00 | No | No | Current |