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
- 63323-088_5863f578-6c6e-4360-abf5-25b6abf62c1c
- Product NDC
- 63323-088
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Sodium Chloride
- Labeler
- Fresenius Kabi USA, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start / end (source format)
- 20010112
- Source listing expiry
- 20261231
Source-listed ingredients
- SODIUM CHLORIDE — 234 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 VIAL, PHARMACY BULK PACKAGE in 1 TRAY (63323-088-61) / 100 mL in 1 VIAL, PHARMACY BULK PACKAGE · 63323-088-61
- 10 VIAL, PHARMACY BULK PACKAGE in 1 TRAY (63323-088-63) / 200 mL in 1 VIAL, PHARMACY BULK PACKAGE · 63323-088-63
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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