United States · FDA National Drug Code directory
CYCLOBENZAPRINE HYDROCHLORIDE
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
- 82804-259_80f88553-aa8f-493a-83df-76055b11f9fc
- Product NDC
- 82804-259
- Form
- TABLET, FILM COATED
- Composition / generic term
- cyclobenzaprine hydrochloride
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170531
- Source listing expiry
- 20271231
Source-listed ingredients
- CYCLOBENZAPRINE HYDROCHLORIDE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 20 TABLET, FILM COATED in 1 BOTTLE (82804-259-20) · 82804-259-20
- 30 TABLET, FILM COATED in 1 BOTTLE (82804-259-30) · 82804-259-30
- 60 TABLET, FILM COATED in 1 BOTTLE (82804-259-60) · 82804-259-60
- 120 TABLET, FILM COATED in 1 BOTTLE (82804-259-72) · 82804-259-72
- 90 TABLET, FILM COATED in 1 BOTTLE (82804-259-90) · 82804-259-90
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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