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
- 63323-186_75c567e3-582b-4fff-9a72-f326f1d13c8f
- Product NDC
- 63323-186
- Form
- INJECTION
- Composition / generic term
- SODIUM CHLORIDE
- Labeler
- Fresenius Kabi USA, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20000810
- Source listing expiry
- 20261231
Source-listed ingredients
- SODIUM CHLORIDE — 9 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 25 VIAL, SINGLE-DOSE in 1 TRAY (63323-186-02) / 2 mL in 1 VIAL, SINGLE-DOSE (63323-186-04) · 63323-186-02
- 25 VIAL, SINGLE-DOSE in 1 TRAY (63323-186-10) / 10 mL in 1 VIAL, SINGLE-DOSE (63323-186-01) · 63323-186-10
- 25 VIAL, SINGLE-DOSE in 1 TRAY (63323-186-20) / 20 mL in 1 VIAL, SINGLE-DOSE (63323-186-03) · 63323-186-20
Source and coverage
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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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