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
- 71205-356_b8f42c39-b984-478f-a2b8-97209a356960
- Product NDC
- 71205-356
- Form
- TABLET, FILM COATED
- Composition / generic term
- cyclobenzaprine hydrochloride
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170531
- Source listing expiry
- 20261231
Source-listed ingredients
- CYCLOBENZAPRINE HYDROCHLORIDE — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 15 TABLET, FILM COATED in 1 BOTTLE (71205-356-15) · 71205-356-15
- 20 TABLET, FILM COATED in 1 BOTTLE (71205-356-20) · 71205-356-20
- 21 TABLET, FILM COATED in 1 BOTTLE (71205-356-21) · 71205-356-21
- 30 TABLET, FILM COATED in 1 BOTTLE (71205-356-30) · 71205-356-30
- 40 TABLET, FILM COATED in 1 BOTTLE (71205-356-40) · 71205-356-40
- 60 TABLET, FILM COATED in 1 BOTTLE (71205-356-60) · 71205-356-60
- 90 TABLET, FILM COATED in 1 BOTTLE (71205-356-90) · 71205-356-90
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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