Cyclobenzaprine Hydrochloride
NDC 69306-015, Cyclobenzaprine Hydrochloride, capsule, extended release, from Doc Rx.
- Product NDC
- 69306-015
- Status
- Listed
- Labeler
- Doc Rx
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA AUTHORIZED GENERIC
- Application
- NDA021777
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/69306-015 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- CYCLOBENZAPRINE HYDROCHLORIDE15 mg/1
Pharmacologic classes
Centrally-mediated Muscle Relaxation [PE]; Muscle Relaxant [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 69306-015-03 | 69306001503 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (69306-015-03) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/d4457b8c-fff8-4c19-8d5a-a667161e5446
Use it
Look up 69306-015 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/69306-015 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 69306-015. 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.