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DEXTROSE AND SODIUM CHLORIDE

NDC 63323-874, DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, injection, solution, from Fresenius Kabi USA, LLC.

Product NDC
63323-874
Status
Listed
Labeler
Fresenius Kabi USA, LLC
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211190
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/63323-874 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DEXTROSE MONOHYDRATE2.5 g/100mL
  • SODIUM CHLORIDE.45 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
63323-874-106332308741010 BAG in 1 CASE (63323-874-10) / 1000 mL in 1 BAG

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b825c9c4-f2fb-4a4a-9d8c-fb020ad07e93

Use it

Look up 63323-874 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63323-874 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63323-874. 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.