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EXTRANEAL

NDC 0941-0681, icodextrin, sodium chloride, sodium lactate, calcium chloride, magnesium chloride, injection, solution, from Vantive US Healthcare LLC.

Product NDC
0941-0681
Status
Listed
Labeler
Vantive US Healthcare LLC
Dosage form
INJECTION, SOLUTION
Route
INTRAPERITONEAL
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/0941-0681 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ICODEXTRIN7.5 g/100mL
  • SODIUM CHLORIDE540 mg/100mL
  • SODIUM LACTATE450 mg/100mL
  • CALCIUM CHLORIDE25.7 mg/100mL
  • MAGNESIUM CHLORIDE5.1 mg/100mL

Pharmacologic classes

Blood Coagulation Factor [EPC]; Calcium [CS]; Calculi Dissolution Agent [EPC]; Cations, Divalent [CS]; Increased Coagulation Factor Activity [PE]; Increased Large Intestinal Motility [PE]; Increased Large Intestinal Motility [PE]; Increased Large Intestinal Motility [PE]; Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]; Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]; Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]; Inhibition Small Intestine Fluid/Electrolyte Absorption [PE]; Magnesium Ion Exchange Activity [MoA]; Osmotic Activity [MoA]; Osmotic Activity [MoA]; Osmotic Activity [MoA]; Osmotic Laxative [EPC]; Osmotic Laxative [EPC]; Osmotic Laxative [EPC]; Phosphate Binder [EPC]; Phosphate Chelating Activity [MoA]; Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]

Package NDCNDC-11Package
0941-0681-04009410681044 BAG in 1 CARTON (0941-0681-04) / 2500 mL in 1 BAG (0941-0681-01)
0941-0681-08009410681084 BAG in 1 CARTON (0941-0681-08) / 2500 mL in 1 BAG (0941-0681-02)

Linked data

RxNorm, label and prices

Use it

Look up 0941-0681 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0941-0681 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0941-0681. 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.