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
- 68788-9967_e381786e-1a5f-4d43-b7d1-3abc16c3dec3
- Product NDC
- 68788-9967
- Form
- TABLET, FILM COATED
- Composition / generic term
- Cyclobenzaprine Hydrochloride
- Labeler
- Preferred Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20150501
- Source listing expiry
- 20271231
Source-listed ingredients
- CYCLOBENZAPRINE HYDROCHLORIDE — 7.5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (68788-9967-1) · 68788-9967-1
- 20 TABLET, FILM COATED in 1 BOTTLE (68788-9967-2) · 68788-9967-2
- 30 TABLET, FILM COATED in 1 BOTTLE (68788-9967-3) · 68788-9967-3
- 60 TABLET, FILM COATED in 1 BOTTLE (68788-9967-6) · 68788-9967-6
- 8 TABLET, FILM COATED in 1 BOTTLE (68788-9967-7) · 68788-9967-7
- 120 TABLET, FILM COATED in 1 BOTTLE (68788-9967-8) · 68788-9967-8
- 90 TABLET, FILM COATED in 1 BOTTLE (68788-9967-9) · 68788-9967-9
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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