United States · FDA National Drug Code directory
CHLORZOXAZONE
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
- 71335-2433_74951b92-2fb8-4a07-9084-5f99f570a40d
- Product NDC
- 71335-2433
- Form
- TABLET
- Composition / generic term
- CHLORZOXAZONE
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220405
- Source listing expiry
- 20261231
Source-listed ingredients
- CHLORZOXAZONE — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 20 TABLET in 1 BOTTLE (71335-2433-1) · 71335-2433-1
- 30 TABLET in 1 BOTTLE (71335-2433-2) · 71335-2433-2
- 40 TABLET in 1 BOTTLE (71335-2433-3) · 71335-2433-3
- 90 TABLET in 1 BOTTLE (71335-2433-4) · 71335-2433-4
- 60 TABLET in 1 BOTTLE (71335-2433-5) · 71335-2433-5
- 100 TABLET in 1 BOTTLE (71335-2433-6) · 71335-2433-6
- 14 TABLET in 1 BOTTLE (71335-2433-7) · 71335-2433-7
- 7 TABLET in 1 BOTTLE (71335-2433-8) · 71335-2433-8
- 120 TABLET in 1 BOTTLE (71335-2433-9) · 71335-2433-9
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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