SUGAMMADEX SODIUM
NDC 42023-830, SUGAMMADEX SODIUM, solution, from Par Health USA, LLC.
- Product NDC
- 42023-830
- Status
- Listed
- Labeler
- Par Health USA, LLC
- Dosage form
- SOLUTION
- Route
- INTRAVENOUS
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA218814
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/42023-830 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SUGAMMADEX SODIUM200 mg/2mL
Pharmacologic classes
gamma-Cyclodextrins [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 42023-830-10 | 42023083010 | 10 SYRINGE in 1 CARTON (42023-830-10) / 2 mL in 1 SYRINGE |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/579a2a1f-4d0c-4851-e063-6294a90a2be6
Use it
Look up 42023-830 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/42023-830 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 42023-830. 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.