United States · FDA National Drug Code directory
Dextrose
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
- 63323-824_0591ab74-99a6-40ee-af96-80bc2ef423dc
- Product NDC
- 63323-824
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Dextrose Monohydrate
- Labeler
- Fresenius Kabi USA, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190329
- Source listing expiry
- 20271231
Source-listed ingredients
- DEXTROSE MONOHYDRATE — 100 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 30 BAG in 1 CASE (63323-824-74) / 250 mL in 1 BAG (63323-824-24) · 63323-824-74
- 20 BAG in 1 CASE (63323-824-75) / 500 mL in 1 BAG (63323-824-25) · 63323-824-75
- 10 BAG in 1 CASE (63323-824-76) / 1000 mL in 1 BAG (63323-824-26) · 63323-824-76
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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