Cyclobenzaprine Hydrochloride
NDC 72603-311, Cyclobenzaprine Hydrochloride, tablet, film coated, from NORTHSTAR RX LLC.
- Product NDC
- 72603-311
- Status
- Listed
- Labeler
- NORTHSTAR RX 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/72603-311 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- CYCLOBENZAPRINE HYDROCHLORIDE7.5 mg/1
Pharmacologic classes
Centrally-mediated Muscle Relaxation [PE]; Muscle Relaxant [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 72603-311-01 | 72603031101 | 100 TABLET, FILM COATED in 1 BOTTLE (72603-311-01) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/2a3a13c3-116c-4e9e-a7f3-7ad7c80486c3NADAC price for package 72603031101
GET /v1/drugs/nadac/72603031101
Use it
Look up 72603-311 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/72603-311 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 72603-311. 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.