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
- 17271-772_c1763362-1955-43ef-a295-c56e1cee5570
- Product NDC
- 17271-772
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Dextrose Monohydrate
- Labeler
- BECTON DICKINSON AND COMPANY
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20161021
- Source listing expiry
- 20271231
Source-listed ingredients
- DEXTROSE MONOHYDRATE — 2500 mg/50mL
These values do not establish equivalence or a dose recommendation.
Packages
- 60 BAG in 1 CASE (17271-772-02) / 50 mL in 1 BAG · 17271-772-02
- 50 BAG in 1 CASE (17271-772-03) / 100 mL in 1 BAG · 17271-772-03
- 30 BAG in 1 CASE (17271-772-05) / 250 mL in 1 BAG · 17271-772-05
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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