Metaxalone
- Product NDC
- 68788-7073
- 11-digit product format
- 687887073
- Labeler code
- 68788
- Product ID
- 68788-7073_e37e2eea-f91f-477d-a287-0e8bbde9aac0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metaxalone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA207466
- Marketing category
- ANDA
- Marketing start
- 2018-01-02
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record