CHLORZOXAZONE
- Product NDC
- 52817-231
- 11-digit product format
- 528170231
- Labeler code
- 52817
- Product ID
- 52817-231_2ea41124-ef4c-4ad1-957f-71c1266ee95f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CHLORZOXAZONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- TruPharma, LLC
- Application
- ANDA212053
- Marketing category
- ANDA
- Marketing start
- 2020-10-12
- 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
- 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 |
|---|
| 52817-231-10 | 52817023110 | 100 TABLET in 1 BOTTLE, PLASTIC (52817-231-10) | 100 tablet | 2020-10-12 | 0000-00-00 | No | No | Current |