Potassium Chloride in Dextrose and Sodium Chloride
NDC 65219-151, DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE, injection, solution, from Fresenius Kabi USA, LLC.
- Product NDC
- 65219-151
- Status
- Listed
- Labeler
- Fresenius Kabi USA, LLC
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA212348
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/65219-151 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- DEXTROSE MONOHYDRATE50 g/1000mL
- SODIUM CHLORIDE2.25 g/1000mL
- POTASSIUM CHLORIDE1.49 g/1000mL
Pharmacologic classes
Increased Large Intestinal Motility [PE]; Increased Large Intestinal Motility [PE]; Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]; Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]; Osmotic Activity [MoA]; Osmotic Activity [MoA]; Osmotic Laxative [EPC]; Osmotic Laxative [EPC]; Potassium Compounds [CS]; Potassium Salt [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 65219-151-75 | 65219015175 | 20 BAG in 1 CASE (65219-151-75) / 500 mL in 1 BAG (65219-151-00) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/f0cc6713-4d47-49be-8116-901c99002b6b
Use it
Look up 65219-151 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/65219-151 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 65219-151. 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.