Cyclobenzaprine Hydrochloride
NDC 0093-1921, Cyclobenzaprine Hydrochloride, capsule, extended release, from Teva Pharmaceuticals USA, Inc..
- Product NDC
- 0093-1921
- Status
- Listed
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA AUTHORIZED GENERIC
- Application
- NDA021777
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/0093-1921 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- CYCLOBENZAPRINE HYDROCHLORIDE30 mg/1
Pharmacologic classes
Centrally-mediated Muscle Relaxation [PE]; Muscle Relaxant [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 0093-1921-06 | 00093192106 | 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-1921-06) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/ca74d27a-f7c6-462d-a913-1cfa061bd8f3NADAC price for package 00093192106
GET /v1/drugs/nadac/00093192106
Use it
Look up 0093-1921 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0093-1921 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0093-1921. 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.