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
- 65219-328_baa9da26-d05b-456b-9b6d-9b154d88d643
- Product NDC
- 65219-328
- Form
- INJECTION, SOLUTION
- Composition / generic term
- SODIUM CHLORIDE
- Labeler
- Fresenius Kabi USA, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170919
- Source listing expiry
- 20271231
Source-listed ingredients
- SODIUM CHLORIDE — 9 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 BAG in 1 CASE (65219-328-50) / 1000 mL in 1 BAG (65219-328-10) · 65219-328-50
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.
Browse United States records →