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Sodium Chloride

NDC 0409-6660, SODIUM CHLORIDE, injection, solution, concentrate, from Hospira, Inc..

Product NDC
0409-6660
Status
Listed
Labeler
Hospira, Inc.
Dosage form
INJECTION, SOLUTION, CONCENTRATE
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA018897
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0409-6660 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM CHLORIDE5.84 g/40mL

Pharmacologic classes

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

Package NDCNDC-11Package
0409-6660-750040966607525 VIAL in 1 TRAY (0409-6660-75) / 40 mL in 1 VIAL (0409-6660-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/018a8807-1331-41c3-4889-c7ec502a9043

Use it

Look up 0409-6660 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0409-6660 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0409-6660. 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.