United States · FDA National Drug Code directory

SODIUM CHLORIDE

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
0338-9159_68658d06-413b-4bd2-8ebc-5513e1e48bba
Product NDC
0338-9159
Form
INJECTION
Composition / generic term
sodium chloride
Labeler
Baxter Healthcare Corporation
Marketing category
NDA
Marketing start / end (source format)
19921207
Source listing expiry
20271231

Source-listed ingredients

  • SODIUM CHLORIDE — 900 mg/100mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 mL in 1 BAG (0338-9159-30) · 0338-9159-30

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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