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
- 71205-426_8a05b052-c0ab-4cb1-af99-1d9c65024412
- Product NDC
- 71205-426
- Form
- TABLET
- Composition / generic term
- Metaxalone
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20161122
- Source listing expiry
- 20261231
Source-listed ingredients
- METAXALONE — 800 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 14 TABLET in 1 BOTTLE (71205-426-14) · 71205-426-14
- 20 TABLET in 1 BOTTLE (71205-426-20) · 71205-426-20
- 30 TABLET in 1 BOTTLE (71205-426-30) · 71205-426-30
- 60 TABLET in 1 BOTTLE (71205-426-60) · 71205-426-60
- 90 TABLET in 1 BOTTLE (71205-426-90) · 71205-426-90
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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