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
- 0338-0085_b4404498-6ab7-4c25-a5a2-5377a6dfecca
- Product NDC
- 0338-0085
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Dextrose and Sodium Chloride
- Labeler
- Baxter Healthcare Company
- Marketing category
- NDA
- Marketing start / end (source format)
- 19710322
- Source listing expiry
- 20261231
Source-listed ingredients
- DEXTROSE MONOHYDRATE — 5 g/100mL
- SODIUM CHLORIDE — 450 mg/100mL
These values do not establish equivalence or a dose recommendation.
Packages
- 24 BAG in 1 CARTON (0338-0085-03) / 500 mL in 1 BAG · 0338-0085-03
- 14 BAG in 1 CARTON (0338-0085-04) / 1000 mL in 1 BAG · 0338-0085-04
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →