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Sodium chloride

NDC 65219-222, SODIUM CHLORIDE, injection, solution, from Fresenius Kabi USA, LLC.

Product NDC
65219-222
Status
Listed
Labeler
Fresenius Kabi USA, LLC
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207310
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65219-222 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM CHLORIDE9 mg/mL

Pharmacologic classes

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

Package NDCNDC-11Package
65219-222-256521902222530 BAG in 1 CASE (65219-222-25) / 250 mL in 1 BAG (65219-222-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d98bf9f7-30ec-4927-a577-cabad192cb18

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=65219-222

Use it

Look up 65219-222 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65219-222 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65219-222. 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.