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
- 17271-721_16de339e-70a9-4375-8e4b-31b6313b6666
- Product NDC
- 17271-721
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Dextrose Monohydrate
- Labeler
- Becton Dickinson and Company
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200205
- 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 (17271-721-05) / 250 mL in 1 BAG · 17271-721-05
- 20 BAG in 1 CASE (17271-721-06) / 500 mL in 1 BAG · 17271-721-06
- 10 BAG in 1 CASE (17271-721-07) / 1000 mL in 1 BAG · 17271-721-07
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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