Dextrose
NDC 65219-240, Dextrose Monohydrate, injection, solution, from Fresenius Kabi USA, LLC.
- Product NDC
- 65219-240
- Status
- Listed
- Labeler
- Fresenius Kabi USA, LLC
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA207449
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/65219-240 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- DEXTROSE MONOHYDRATE25000 mg/500mL
| Package NDC | NDC-11 | Package |
|---|---|---|
| 65219-240-50 | 65219024050 | 20 BAG in 1 CASE (65219-240-50) / 500 mL in 1 BAG (65219-240-01) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/bd250a46-d229-4e80-b5a1-b34169ccecc4Medicare Part B payment limits (ASP)
GET /v1/drugs/asp?ndc=65219-240
Use it
Look up 65219-240 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/65219-240 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 65219-240. 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.