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
- 71335-2066_9774fc12-2fd3-4928-8960-6a211eabfb68
- Product NDC
- 71335-2066
- Form
- TABLET
- Composition / generic term
- Metaxalone
- Labeler
- Bryant Ranch Prepack
- 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
- 30 TABLET in 1 BOTTLE (71335-2066-1) · 71335-2066-1
- 90 TABLET in 1 BOTTLE (71335-2066-2) · 71335-2066-2
- 100 TABLET in 1 BOTTLE (71335-2066-3) · 71335-2066-3
- 60 TABLET in 1 BOTTLE (71335-2066-4) · 71335-2066-4
- 10 TABLET in 1 BOTTLE (71335-2066-5) · 71335-2066-5
- 20 TABLET in 1 BOTTLE (71335-2066-6) · 71335-2066-6
- 120 TABLET in 1 BOTTLE (71335-2066-7) · 71335-2066-7
- 15 TABLET in 1 BOTTLE (71335-2066-8) · 71335-2066-8
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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