Cyclobenzaprine Hydrochloride
NDC 72789-036, cyclobenzaprine hydrochloride, tablet, film coated, from PD-Rx Pharmaceuticals, Inc..
- Product NDC
- 72789-036
- Status
- Listed
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA077797
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/72789-036 \ -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 |
|---|---|---|
| 72789-036-01 | 72789003601 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-036-01) |
| 72789-036-15 | 72789003615 | 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-036-15) |
| 72789-036-21 | 72789003621 | 21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-036-21) |
| 72789-036-30 | 72789003630 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-036-30) |
| 72789-036-45 | 72789003645 | 45 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-036-45) |
| 72789-036-60 | 72789003660 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-036-60) |
| 72789-036-82 | 72789003682 | 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-036-82) |
| 72789-036-90 | 72789003690 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-036-90) |
| 72789-036-93 | 72789003693 | 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-036-93) |
| 72789-036-94 | 72789003694 | 270 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-036-94) |
| 72789-036-95 | 72789003695 | 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-036-95) |
| 72789-036-98 | 72789003698 | 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-036-98) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/3aaa4808-7f2d-410c-9b6c-193549ec0845
Use it
Look up 72789-036 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/72789-036 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 72789-036. 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.