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
- 63187-812_3afe19fb-b693-47f7-a08e-a46cc756ffda
- Product NDC
- 63187-812
- Form
- TABLET, FILM COATED
- Composition / generic term
- Cyclobenzaprine
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160722
- 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 (63187-812-07) · 63187-812-07
- 10 TABLET, FILM COATED in 1 BOTTLE (63187-812-10) · 63187-812-10
- 12 TABLET, FILM COATED in 1 BOTTLE (63187-812-12) · 63187-812-12
- 15 TABLET, FILM COATED in 1 BOTTLE (63187-812-15) · 63187-812-15
- 20 TABLET, FILM COATED in 1 BOTTLE (63187-812-20) · 63187-812-20
- 21 TABLET, FILM COATED in 1 BOTTLE (63187-812-21) · 63187-812-21
- 30 TABLET, FILM COATED in 1 BOTTLE (63187-812-30) · 63187-812-30
- 45 TABLET, FILM COATED in 1 BOTTLE (63187-812-45) · 63187-812-45
- 60 TABLET, FILM COATED in 1 BOTTLE (63187-812-60) · 63187-812-60
- 120 TABLET, FILM COATED in 1 BOTTLE (63187-812-72) · 63187-812-72
- 90 TABLET, FILM COATED in 1 BOTTLE (63187-812-90) · 63187-812-90
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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