Cyclobenzaprine Hydrochloride
NDC 70518-4225, Cyclobenzaprine Hydrochloride, capsule, extended release, from REMEDYREPACK INC..
- Product NDC
- 70518-4225
- Status
- Listed
- Labeler
- REMEDYREPACK INC.
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA091281
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4225 \ -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 |
|---|---|---|
| 70518-4225-0 | 70518422500 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4225-0) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/ba659e1a-0091-45f6-b418-f4f36c9a2c79
Use it
Look up 70518-4225 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4225 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70518-4225. 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.