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Dextrose and Sodium Chloride

NDC 17271-734, DEXTROSE MONOHYDRATE and SODIUM CHLORIDE, injection, solution, from BECTON DICKINSON AND COMPANY.

Product NDC
17271-734
Status
Listed
Labeler
BECTON DICKINSON AND COMPANY
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/17271-734 \
  -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
17271-734-051727107340530 BAG in 1 CASE (17271-734-05) / 250 mL in 1 BAG
17271-734-061727107340620 BAG in 1 CASE (17271-734-06) / 500 mL in 1 BAG
17271-734-071727107340710 BAG in 1 CASE (17271-734-07) / 1000 mL in 1 BAG

Linked data

RxNorm, label and prices

Use it

Look up 17271-734 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/17271-734 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 17271-734. 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.