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
- 68788-4154_84be93c5-1526-465e-ab0b-c6d10ba1521d
- Product NDC
- 68788-4154
- Form
- TABLET, FILM COATED
- Composition / generic term
- Cyclobenzaprine Hydrochloride
- Labeler
- Preferred Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260715
- 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 (68788-4154-2) · 68788-4154-2
- 30 TABLET, FILM COATED in 1 BOTTLE (68788-4154-3) · 68788-4154-3
- 15 TABLET, FILM COATED in 1 BOTTLE (68788-4154-5) · 68788-4154-5
- 60 TABLET, FILM COATED in 1 BOTTLE (68788-4154-6) · 68788-4154-6
- 90 TABLET, FILM COATED in 1 BOTTLE (68788-4154-9) · 68788-4154-9
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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