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Glucose and Sodium Chloride

NDC 0338-9799, Dextrose Anhydrous and Sodium Chloride, injection, solution, from Baxter Healthcare Corporation.

Product NDC
0338-9799
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/0338-9799 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DEXTROSE MONOHYDRATE5.5 g/100mL
  • 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
0338-9799-120033897991212 BAG in 1 CARTON (0338-9799-12) / 1000 mL in 1 BAG (0338-9799-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1ba918d0-13d0-48bc-8742-658fc0eb47b6

Use it

Look up 0338-9799 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0338-9799 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0338-9799. 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.