United States · FDA National Drug Code directory
Metaxalone
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 68788-7675_a6b814fb-1fc1-4ba0-bde1-7ba001706595
- Product NDC
- 68788-7675
- Form
- TABLET
- Composition / generic term
- Metaxalone
- Labeler
- Preferred Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200302
- Source listing expiry
- 20271231
Source-listed ingredients
- METAXALONE — 800 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 15 TABLET in 1 BOTTLE (68788-7675-0) · 68788-7675-0
- 100 TABLET in 1 BOTTLE (68788-7675-1) · 68788-7675-1
- 20 TABLET in 1 BOTTLE (68788-7675-2) · 68788-7675-2
- 30 TABLET in 1 BOTTLE (68788-7675-3) · 68788-7675-3
- 60 TABLET in 1 BOTTLE (68788-7675-6) · 68788-7675-6
- 90 TABLET in 1 BOTTLE (68788-7675-9) · 68788-7675-9
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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