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Sodium chloride

NDC 65219-502, SODIUM CHLORIDE, injection, solution, from Fresenius Kabi USA, LLC.

Product NDC
65219-502
Status
Listed
Labeler
Fresenius Kabi USA, LLC
Dosage form
INJECTION, SOLUTION
Route
IRRIGATION
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213688
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65219-502 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM CHLORIDE.9 g/100mL

Pharmacologic classes

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

Package NDCNDC-11Package
65219-502-10652190502106 BAG in 1 CASE (65219-502-10) / 1000 mL in 1 BAG (65219-502-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ce0c8c6f-734a-400f-9b60-a3b1e263f25f

Use it

Look up 65219-502 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65219-502 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65219-502. 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.