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
- 72189-080_2be81315-9d30-1301-e063-6394a90a6a84
- Product NDC
- 72189-080
- Form
- TABLET, FILM COATED
- Composition / generic term
- CYCLOBENZAPRINE HYDROCHLORIDE
- Labeler
- DIRECT RX
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200513
- Source listing expiry
- 20261231
Source-listed ingredients
- CYCLOBENZAPRINE HYDROCHLORIDE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 7 TABLET, FILM COATED in 1 BOTTLE (72189-080-07) · 72189-080-07
- 10 TABLET, FILM COATED in 1 BOTTLE (72189-080-10) · 72189-080-10
- 15 TABLET, FILM COATED in 1 BOTTLE (72189-080-15) · 72189-080-15
- 20 TABLET, FILM COATED in 1 BOTTLE (72189-080-20) · 72189-080-20
- 21 TABLET, FILM COATED in 1 BOTTLE (72189-080-21) · 72189-080-21
- 30 TABLET, FILM COATED in 1 BOTTLE (72189-080-30) · 72189-080-30
- 45 TABLET, FILM COATED in 1 BOTTLE (72189-080-45) · 72189-080-45
- 60 TABLET, FILM COATED in 1 BOTTLE (72189-080-60) · 72189-080-60
- 120 TABLET, FILM COATED in 1 BOTTLE (72189-080-72) · 72189-080-72
- 90 TABLET, FILM COATED in 1 BOTTLE (72189-080-90) · 72189-080-90
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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