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
- 63323-623_b9f9ae0e-b72d-480a-b1cc-41d817aa83be
- Product NDC
- 63323-623
- 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
- 20261231
Source-listed ingredients
- SODIUM CHLORIDE — 9 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 50 mL in 1 BAG (63323-623-53) · 63323-623-53
- 100 mL in 1 BAG (63323-623-61) · 63323-623-61
- 250 mL in 1 BAG (63323-623-74) · 63323-623-74
- 500 mL in 1 BAG (63323-623-75) · 63323-623-75
- 1000 mL in 1 BAG (63323-623-76) · 63323-623-76
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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