VECURONIUM BROMIDE
NDC 51662-1707, VECURONIUM BROMIDE, injection, powder, for solution, from HF Acquisition Co LLC, DBA HealthFirst.
- Product NDC
- 51662-1707
- Status
- Listed
- Labeler
- HF Acquisition Co LLC, DBA HealthFirst
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAVENOUS
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA203725
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/51662-1707 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- VECURONIUM BROMIDE10 mg/1
Pharmacologic classes
Neuromuscular Nondepolarizing Blockade [PE]; Nondepolarizing Neuromuscular Blocker [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 51662-1707-1 | 51662170701 | 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (51662-1707-1) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/582c7f44-b614-18df-e063-6294a90a74b6
Use it
Look up 51662-1707 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/51662-1707 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 51662-1707. 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.