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
- 17271-734_cfe5e2b2-fe4e-4fa2-9dee-3197ac1de46d
- Product NDC
- 17271-734
- Form
- INJECTION, SOLUTION
- Composition / generic term
- DEXTROSE MONOHYDRATE and SODIUM CHLORIDE
- Labeler
- BECTON DICKINSON AND COMPANY
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20201026
- Source listing expiry
- 20261231
Source-listed ingredients
- DEXTROSE MONOHYDRATE — 5 g/100mL
- SODIUM CHLORIDE — .45 g/100mL
These values do not establish equivalence or a dose recommendation.
Packages
- 30 BAG in 1 CASE (17271-734-05) / 250 mL in 1 BAG · 17271-734-05
- 20 BAG in 1 CASE (17271-734-06) / 500 mL in 1 BAG · 17271-734-06
- 10 BAG in 1 CASE (17271-734-07) / 1000 mL in 1 BAG · 17271-734-07
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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