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Sodium chloride

NDC 65219-230, SODIUM CHLORIDE, injection, solution, from Fresenius Kabi USA, LLC.

Product NDC
65219-230
Status
Listed
Labeler
Fresenius Kabi USA, LLC
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208122
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65219-230 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM CHLORIDE1125 mg/250mL

Pharmacologic classes

Increased Large Intestinal Motility [PE]; Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]; Osmotic Activity [MoA]; Osmotic Laxative [EPC]

Package NDCNDC-11Package
65219-230-256521902302530 BAG in 1 CASE (65219-230-25) / 250 mL in 1 BAG (65219-230-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/239a5af1-7498-480f-862c-ab7c3d89d183

Use it

Look up 65219-230 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65219-230 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65219-230. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.