CYCLOBENZAPRINE HYDROCHLORIDE
NDC 82804-259, cyclobenzaprine hydrochloride, tablet, film coated, from Proficient Rx LP.
- Product NDC
- 82804-259
- Status
- Listed
- Labeler
- Proficient Rx LP
- 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/82804-259 \ -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 |
|---|---|---|
| 82804-259-20 | 82804025920 | 20 TABLET, FILM COATED in 1 BOTTLE (82804-259-20) |
| 82804-259-30 | 82804025930 | 30 TABLET, FILM COATED in 1 BOTTLE (82804-259-30) |
| 82804-259-60 | 82804025960 | 60 TABLET, FILM COATED in 1 BOTTLE (82804-259-60) |
| 82804-259-72 | 82804025972 | 120 TABLET, FILM COATED in 1 BOTTLE (82804-259-72) |
| 82804-259-90 | 82804025990 | 90 TABLET, FILM COATED in 1 BOTTLE (82804-259-90) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/dfe7288c-a477-4f32-a9ab-00cc981a1a57
Use it
Look up 82804-259 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/82804-259 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 82804-259. 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.