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
- 63323-099_f5197532-af45-42c9-919b-30d00276650e
- Product NDC
- 63323-099
- Form
- INJECTION, SOLUTION, CONCENTRATE
- Composition / generic term
- Sodium Chloride
- Labeler
- Fresenius Kabi USA, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230711
- Source listing expiry
- 20261231
Source-listed ingredients
- SODIUM CHLORIDE — 4 meq/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 VIAL, PLASTIC in 1 TRAY (63323-099-63) / 200 mL in 1 VIAL, PLASTIC (63323-099-03) · 63323-099-63
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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