United States · FDA National Drug Code directory
Potassium Chloride in 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
- 0338-0807_bd6aeaeb-f4ba-417c-ba5f-0b47a9d47e8b
- Product NDC
- 0338-0807
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Potassium Chloride, Dextrose Monohydrate and Sodium Chloride
- Labeler
- Baxter Healthcare Company
- Marketing category
- NDA
- Marketing start / end (source format)
- 19850405
- Source listing expiry
- 20271231
Source-listed ingredients
- POTASSIUM CHLORIDE — 300 mg/100mL
- DEXTROSE MONOHYDRATE — 5 g/100mL
- SODIUM CHLORIDE — 900 mg/100mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 mL in 1 BAG (0338-0807-04) · 0338-0807-04
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 →