Chlorzoxazone
- Product NDC
- 70518-0496
- 11-digit product format
- 705180496
- Labeler code
- 70518
- Product ID
- 70518-0496_e1e03004-da19-6018-e053-2a95a90ad900
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorzoxazone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA089859
- Marketing category
- ANDA
- Marketing start
- 2017-11-15
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 70518-0496-1 | 70518049601 | 30 TABLET in 1 BOTTLE, PLASTIC (70518-0496-1) | 30 tablet | 2019-12-02 | 0000-00-00 | No | No | Current |
| 70518-0496-2 | 70518049602 | 20 TABLET in 1 BOTTLE, PLASTIC (70518-0496-2) | 20 tablet | 2020-06-18 | 0000-00-00 | No | No | Current |