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Sodium chloride

NDC 17271-771, SODIUM CHLORIDE, injection, solution, from BECTON DICKINSON AND COMPANY.

Product NDC
17271-771
Status
Listed
Labeler
BECTON DICKINSON AND COMPANY
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207310
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/17271-771 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM CHLORIDE9 mg/mL

Pharmacologic classes

Increased Large Intestinal Motility [PE]; Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]; Osmotic Activity [MoA]; Osmotic Laxative [EPC]

Package NDCNDC-11Package
17271-771-021727107710260 BAG in 1 CASE (17271-771-02) / 50 mL in 1 BAG
17271-771-031727107710350 BAG in 1 CASE (17271-771-03) / 100 mL in 1 BAG
17271-771-051727107710530 BAG in 1 CASE (17271-771-05) / 250 mL in 1 BAG

Linked data

RxNorm, label and prices

Use it

Look up 17271-771 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/17271-771 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 17271-771. 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.