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
- 76420-599_04ab2bbb-1be5-1bfc-e063-6394a90a103e
- Product NDC
- 76420-599
- Form
- TABLET, FILM COATED
- Composition / generic term
- Cyclobenzaprine Hydrochloride
- Labeler
- Asclemed USA, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20080926
- Source listing expiry
- 20261231
Source-listed ingredients
- CYCLOBENZAPRINE HYDROCHLORIDE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 2 TABLET, FILM COATED in 1 BOTTLE (76420-599-02) · 76420-599-02
- 5 TABLET, FILM COATED in 1 BOTTLE (76420-599-05) · 76420-599-05
- 7 TABLET, FILM COATED in 1 BOTTLE (76420-599-07) · 76420-599-07
- 100 TABLET, FILM COATED in 1 BOTTLE (76420-599-10) · 76420-599-10
- 14 TABLET, FILM COATED in 1 BOTTLE (76420-599-14) · 76420-599-14
- 20 TABLET, FILM COATED in 1 BOTTLE (76420-599-20) · 76420-599-20
- 30 TABLET, FILM COATED in 1 BOTTLE (76420-599-30) · 76420-599-30
- 60 TABLET, FILM COATED in 1 BOTTLE (76420-599-60) · 76420-599-60
- 90 TABLET, FILM COATED in 1 BOTTLE (76420-599-90) · 76420-599-90
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →