United States · FDA National Drug Code directory
DEXTROSE AND 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
- 63323-874_246065b3-688f-43b6-b847-9ba16ac639d4
- Product NDC
- 63323-874
- Form
- INJECTION, SOLUTION
- Composition / generic term
- DEXTROSE MONOHYDRATE, SODIUM CHLORIDE
- Labeler
- Fresenius Kabi USA, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210301
- Source listing expiry
- 20261231
Source-listed ingredients
- DEXTROSE MONOHYDRATE — 2.5 g/100mL
- SODIUM CHLORIDE — .45 g/100mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 BAG in 1 CASE (63323-874-10) / 1000 mL in 1 BAG · 63323-874-10
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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