Chlorzoxazone
- Product NDC
- 70518-2053
- 11-digit product format
- 705182053
- Labeler code
- 70518
- Product ID
- 70518-2053_d6a557e7-2e35-21f2-e053-2995a90ab1a0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorzoxazone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA089859
- Marketing category
- ANDA
- Marketing start
- 2019-05-01
- 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 |
|---|
| 70518-2053-2 | 70518205302 | 25 TABLET in 1 BOTTLE, PLASTIC (70518-2053-2) | 25 tablet | 2020-12-03 | 0000-00-00 | No | No | Current |