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
- 71335-0096_74ade2d7-286b-45e1-ad98-19c4235d4c7b
- Product NDC
- 71335-0096
- Form
- TABLET, FILM COATED
- Composition / generic term
- Cyclobenzaprine Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20150325
- Source listing expiry
- 20261231
Source-listed ingredients
- CYCLOBENZAPRINE HYDROCHLORIDE — 7.5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 TABLET, FILM COATED in 1 BOTTLE (71335-0096-0) · 71335-0096-0
- 60 TABLET, FILM COATED in 1 BOTTLE (71335-0096-1) · 71335-0096-1
- 30 TABLET, FILM COATED in 1 BOTTLE (71335-0096-2) · 71335-0096-2
- 90 TABLET, FILM COATED in 1 BOTTLE (71335-0096-3) · 71335-0096-3
- 120 TABLET, FILM COATED in 1 BOTTLE (71335-0096-4) · 71335-0096-4
- 15 TABLET, FILM COATED in 1 BOTTLE (71335-0096-5) · 71335-0096-5
- 45 TABLET, FILM COATED in 1 BOTTLE (71335-0096-6) · 71335-0096-6
- 9 TABLET, FILM COATED in 1 BOTTLE (71335-0096-7) · 71335-0096-7
- 180 TABLET, FILM COATED in 1 BOTTLE (71335-0096-8) · 71335-0096-8
- 14 TABLET, FILM COATED in 1 BOTTLE (71335-0096-9) · 71335-0096-9
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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