Rocuronium Bromide
NDC 71839-142, rocuronium bromide, injection, solution, from BE Pharmaceuticals Inc..
- Product NDC
- 71839-142
- Status
- Listed
- Labeler
- BE Pharmaceuticals Inc.
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA216234
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71839-142 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- ROCURONIUM BROMIDE10 mg/mL
Pharmacologic classes
Neuromuscular Nondepolarizing Blockade [PE]; Nondepolarizing Neuromuscular Blocker [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 71839-142-10 | 71839014210 | 10 VIAL, MULTI-DOSE in 1 CARTON (71839-142-10) / 10 mL in 1 VIAL, MULTI-DOSE (71839-142-01) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/1543ea2b-54ab-4088-a72a-5d71854a2dce
Use it
Look up 71839-142 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71839-142 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71839-142. 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.