Metaxalone
- Product NDC
- 72789-122
- 11-digit product format
- 727890122
- Labeler code
- 72789
- Product ID
- 72789-122_e66027e0-54d1-70be-e053-2a95a90ab6ab
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metaxalone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA208774
- Marketing category
- ANDA
- Marketing start
- 2018-09-24
- Marketing end
- 0000-00-00
- Substance
- METAXALONE
- Active strength
- 800 mg/1
- Pharmacologic classes
- Centrally-mediated Muscle Relaxation [PE]
- 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 |
|---|
| 72789-122-30 | 72789012230 | 90 TABLET in 1 BOTTLE, PLASTIC (72789-122-30) | 90 tablet | 2020-09-25 | 0000-00-00 | No | No | Current |