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
- 63323-624_40c07bed-7ccc-4117-a595-78c2a053e8a9
- Product NDC
- 63323-624
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Dextrose Monohydrate
- Labeler
- Fresenius Kabi USA, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20161021
- Source listing expiry
- 20261231
Source-listed ingredients
- DEXTROSE MONOHYDRATE — 50 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 BAG in 1 CASE (63323-624-10) / 1000 mL in 1 BAG (63323-624-03) · 63323-624-10
- 60 BAG in 1 CASE (63323-624-50) / 50 mL in 1 BAG (63323-624-05) · 63323-624-50
- 50 BAG in 1 CASE (63323-624-61) / 100 mL in 1 BAG (63323-624-06) · 63323-624-61
- 30 BAG in 1 CASE (63323-624-74) / 250 mL in 1 BAG (63323-624-04) · 63323-624-74
- 20 BAG in 1 CASE (63323-624-75) / 500 mL in 1 BAG (63323-624-07) · 63323-624-75
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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