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
- 63323-873_4ea28693-a341-402a-a8fa-b2a208ae6ab1
- Product NDC
- 63323-873
- Form
- INJECTION, SOLUTION
- Composition / generic term
- DEXTROSE MONOHYDRATE and SODIUM CHLORIDE
- Labeler
- Fresenius Kabi USA, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20201026
- Source listing expiry
- 20271231
Source-listed ingredients
- DEXTROSE MONOHYDRATE — 5 g/100mL
- SODIUM CHLORIDE — .225 g/100mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 BAG in 1 CASE (63323-873-10) / 1000 mL in 1 BAG (63323-873-01) · 63323-873-10
- 20 BAG in 1 CASE (63323-873-74) / 500 mL in 1 BAG (63323-873-05) · 63323-873-74
- 30 BAG in 1 CASE (63323-873-75) / 250 mL in 1 BAG (63323-873-15) · 63323-873-75
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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