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
- 76420-033_f5f82b93-a80e-3ab8-e053-2995a90a68f5
- Product NDC
- 76420-033
- Form
- TABLET, FILM COATED
- Composition / generic term
- cyclobenzaprine hydrochloride
- Labeler
- Asclemed USA, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170330
- 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, PLASTIC (76420-033-01) · 76420-033-01
- 2 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-033-02) · 76420-033-02
- 7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-033-07) · 76420-033-07
- 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-033-20) · 76420-033-20
- 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-033-30) · 76420-033-30
- 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-033-60) · 76420-033-60
- 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-033-90) · 76420-033-90
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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