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Sodium chloride

NDC 17271-701, SODIUM CHLORIDE, injection, solution, from Becton Dickinson and Company.

Product NDC
17271-701
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/17271-701 \
  -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
17271-701-021727107010250 mL in 1 BAG (17271-701-02)
17271-701-0317271070103100 mL in 1 BAG (17271-701-03)
17271-701-0517271070105250 mL in 1 BAG (17271-701-05)
17271-701-0617271070106500 mL in 1 BAG (17271-701-06)
17271-701-07172710701071000 mL in 1 BAG (17271-701-07)

Linked data

RxNorm, label and prices

Use it

Look up 17271-701 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/17271-701 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 17271-701. 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.