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Dextrose and Sodium Chloride

NDC 63323-867, DEXTROSE MONOHYDRATE and SODIUM CHLORIDE, injection, solution, from Fresenius Kabi USA, LLC.

Product NDC
63323-867
Status
Listed
Labeler
Fresenius Kabi USA, LLC
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211194
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/63323-867 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DEXTROSE MONOHYDRATE5 g/100mL
  • SODIUM CHLORIDE.3 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
63323-867-106332308671010 BAG in 1 CASE (63323-867-10) / 1000 mL in 1 BAG
63323-867-746332308677420 BAG in 1 CASE (63323-867-74) / 500 mL in 1 BAG
63323-867-756332308677530 BAG in 1 CASE (63323-867-75) / 250 mL in 1 BAG

Linked data

RxNorm, label and prices

Use it

Look up 63323-867 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63323-867 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63323-867. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.