Metaxalone
- Product NDC
- 68788-6466
- 11-digit product format
- 687886466
- Labeler code
- 68788
- Product ID
- 68788-6466_b94f7bc1-a8bd-4bbd-99b0-a8358e6cac70
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metaxalone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA040445
- Marketing category
- ANDA
- Marketing start
- 2016-08-02
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record