Chlorzoxazone
- Product NDC
- 73007-013
- 11-digit product format
- 730070013
- Labeler code
- 73007
- Product ID
- 73007-013_ec6fa2fe-3dd3-1b94-e053-2a95a90a10a8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorzoxazone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AXIS Pharmaceutics Inc
- Application
- ANDA212254
- Marketing category
- ANDA
- Marketing start
- 2020-01-22
- 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
- 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 |
|---|
| 73007-013-03 | 73007001303 | 100 TABLET in 1 BOTTLE (73007-013-03) | 100 tablet | 2020-01-22 | 0000-00-00 | No | No | Current |
| 73007-013-04 | 73007001304 | 2 BOTTLE in 1 PACKAGE (73007-013-04) > 100 TABLET in 1 BOTTLE | 2 bottle | 2020-01-22 | 0000-00-00 | No | No | Current |