CYCLOBENZAPRINE HYDROCHLORIDE
NDC 51655-592, cyclobenzaprine hydrochloride, tablet, film coated, from Northwind Health Company, LLC.
- Product NDC
- 51655-592
- Status
- Listed
- Labeler
- Northwind Health Company, LLC
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA208170
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/51655-592 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- CYCLOBENZAPRINE HYDROCHLORIDE10 mg/1
Pharmacologic classes
Centrally-mediated Muscle Relaxation [PE]; Muscle Relaxant [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 51655-592-20 | 51655059220 | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-592-20) |
| 51655-592-25 | 51655059225 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-592-25) |
| 51655-592-26 | 51655059226 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-592-26) |
| 51655-592-52 | 51655059252 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-592-52) |
| 51655-592-53 | 51655059253 | 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-592-53) |
| 51655-592-54 | 51655059254 | 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-592-54) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/f32bceda-1d24-322d-e053-2995a90aae1b
Use it
Look up 51655-592 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/51655-592 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 51655-592. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.