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
- 76420-271_e7bfa09d-7e18-d2bf-e053-2995a90a9145
- Product NDC
- 76420-271
- Form
- TABLET, FILM COATED
- Composition / generic term
- Cyclobenzaprine Hydrochloride
- Labeler
- Asclemed USA, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210720
- Source listing expiry
- 20261231
Source-listed ingredients
- CYCLOBENZAPRINE HYDROCHLORIDE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TABLET, FILM COATED in 1 BOTTLE (76420-271-01) · 76420-271-01
- 2 TABLET, FILM COATED in 1 BOTTLE (76420-271-02) · 76420-271-02
- 7 TABLET, FILM COATED in 1 BOTTLE (76420-271-07) · 76420-271-07
- 100 TABLET, FILM COATED in 1 BOTTLE (76420-271-10) · 76420-271-10
- 120 TABLET, FILM COATED in 1 BOTTLE (76420-271-12) · 76420-271-12
- 15 TABLET, FILM COATED in 1 BOTTLE (76420-271-15) · 76420-271-15
- 20 TABLET, FILM COATED in 1 BOTTLE (76420-271-20) · 76420-271-20
- 30 TABLET, FILM COATED in 1 BOTTLE (76420-271-30) · 76420-271-30
- 60 TABLET, FILM COATED in 1 BOTTLE (76420-271-60) · 76420-271-60
- 90 TABLET, FILM COATED in 1 BOTTLE (76420-271-90) · 76420-271-90
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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