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Dextrose and Sodium Chloride

NDC 63323-869, DEXTROSE MONOHYDRATE and SODIUM CHLORIDE, injection, solution, from Fresenius Kabi USA, LLC.

Product NDC
63323-869
Status
Listed
Labeler
Fresenius Kabi USA, LLC
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211276
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/63323-869 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DEXTROSE MONOHYDRATE5 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
63323-869-106332308691010 BAG in 1 CASE (63323-869-10) / 1000 mL in 1 BAG (63323-869-01)
63323-869-746332308697420 BAG in 1 CASE (63323-869-74) / 500 mL in 1 BAG (63323-869-04)
63323-869-756332308697530 BAG in 1 CASE (63323-869-75) / 250 mL in 1 BAG (63323-869-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3c5f0f65-8a54-4a55-ad4e-0f0be97631d7

Use it

Look up 63323-869 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63323-869 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63323-869. 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.