Metaxalone
- Product NDC
- 70518-1161
- 11-digit product format
- 705181161
- Labeler code
- 70518
- Product ID
- 70518-1161_9085e749-92fa-437e-e053-2a95a90ac5cd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metaxalone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- NDA013217
- Marketing category
- NDA
- Marketing start
- 2018-05-07
- 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