Cyclobenzaprine Hydrochloride
NDC 68071-3154, Cyclobenzaprine, tablet, film coated, from NuCare Pharmaceuticals, Inc..
- Product NDC
- 68071-3154
- Status
- Listed
- Labeler
- NuCare Pharmaceuticals, Inc.
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA090478
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/68071-3154 \ -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 |
|---|---|---|
| 68071-3154-1 | 68071315401 | 10 TABLET, FILM COATED in 1 BOTTLE (68071-3154-1) |
| 68071-3154-3 | 68071315403 | 30 TABLET, FILM COATED in 1 BOTTLE (68071-3154-3) |
| 68071-3154-6 | 68071315406 | 6 TABLET, FILM COATED in 1 BOTTLE (68071-3154-6) |
| 68071-3154-7 | 68071315407 | 7 TABLET, FILM COATED in 1 BOTTLE (68071-3154-7) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/4fbbc5b6-7aac-34e5-e054-00144ff88e88
Use it
Look up 68071-3154 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/68071-3154 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 68071-3154. 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.