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
- 63187-590_dfd6a8bf-5460-47a3-9865-ec043cd9d17e
- Product NDC
- 63187-590
- Form
- TABLET, FILM COATED
- Composition / generic term
- Cyclobenzaprine Hydrochloride
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20150325
- Source listing expiry
- 20271231
Source-listed ingredients
- CYCLOBENZAPRINE HYDROCHLORIDE — 7.5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 9 TABLET, FILM COATED in 1 BOTTLE (63187-590-09) · 63187-590-09
- 14 TABLET, FILM COATED in 1 BOTTLE (63187-590-14) · 63187-590-14
- 20 TABLET, FILM COATED in 1 BOTTLE (63187-590-20) · 63187-590-20
- 30 TABLET, FILM COATED in 1 BOTTLE (63187-590-30) · 63187-590-30
- 60 TABLET, FILM COATED in 1 BOTTLE (63187-590-60) · 63187-590-60
- 120 TABLET, FILM COATED in 1 BOTTLE (63187-590-72) · 63187-590-72
- 90 TABLET, FILM COATED in 1 BOTTLE (63187-590-90) · 63187-590-90
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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