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Sodium Chloride

NDC 0338-9804, Sodium Chloride, injection, solution, from Baxter Healthcare Corporation.

Product NDC
0338-9804
Status
Listed
Labeler
Baxter Healthcare Corporation
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE
Application
—
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0338-9804 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM CHLORIDE9 g/1000mL

Pharmacologic classes

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

Package NDCNDC-11Package

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/aaab14e7-a4b4-4b2b-8d73-ba688064a9b1

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=0338-9804

Use it

Look up 0338-9804 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0338-9804 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0338-9804. 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.