CYCLOBENZAPRINE HYDROCHLORIDE
NDC 71205-356, cyclobenzaprine hydrochloride, tablet, film coated, from Proficient Rx LP.
- Product NDC
- 71205-356
- 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/71205-356 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- CYCLOBENZAPRINE HYDROCHLORIDE5 mg/1
Pharmacologic classes
Centrally-mediated Muscle Relaxation [PE]; Muscle Relaxant [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 71205-356-15 | 71205035615 | 15 TABLET, FILM COATED in 1 BOTTLE (71205-356-15) |
| 71205-356-20 | 71205035620 | 20 TABLET, FILM COATED in 1 BOTTLE (71205-356-20) |
| 71205-356-21 | 71205035621 | 21 TABLET, FILM COATED in 1 BOTTLE (71205-356-21) |
| 71205-356-30 | 71205035630 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-356-30) |
| 71205-356-40 | 71205035640 | 40 TABLET, FILM COATED in 1 BOTTLE (71205-356-40) |
| 71205-356-60 | 71205035660 | 60 TABLET, FILM COATED in 1 BOTTLE (71205-356-60) |
| 71205-356-90 | 71205035690 | 90 TABLET, FILM COATED in 1 BOTTLE (71205-356-90) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/34ff8a08-0177-451f-9dbc-e21582346196
Use it
Look up 71205-356 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71205-356 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71205-356. 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.