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3% Sodium Chloride

NDC 17271-703, 3% Sodium Chloride, injection, solution, from Becton Dickinson and Company.

Product NDC
17271-703
Status
Listed
Labeler
Becton Dickinson and Company
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA209476
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/17271-703 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM CHLORIDE3 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
17271-703-061727107030620 BAG in 1 CASE (17271-703-06) / 500 mL in 1 BAG

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a8058593-48af-457a-b0f0-166935c7d10c

Use it

Look up 17271-703 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/17271-703 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 17271-703. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.