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: 55700-239_0498b9cc-1111-40b9-9605-08c32d167c7f
Product NDC: 55700-239
Form: TABLET, FILM COATED
Composition / generic term: Cyclobenzaprine Hydrochloride
Labeler: Quality Care Products LLC
Marketing category: ANDA
Marketing start / end (source format): 20150325 / 20271231

Source-listed ingredients

CYCLOBENZAPRINE HYDROCHLORIDE — 7.5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

90 TABLET, FILM COATED in 1 BOTTLE (55700-239-90) · 55700-239-90

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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