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
- 65219-150_93737cd2-f9e0-41e1-9263-2c4ff516395a
- Product NDC
- 65219-150
- Form
- INJECTION, SOLUTION
- Composition / generic term
- DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE
- Labeler
- Fresenius Kabi USA, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220826
- Source listing expiry
- 20261231
Source-listed ingredients
- DEXTROSE MONOHYDRATE — 25 g/500mL
- SODIUM CHLORIDE — 2.25 g/500mL
- POTASSIUM CHLORIDE — .745 g/500mL
These values do not establish equivalence or a dose recommendation.
Packages
- 20 BAG in 1 CASE (65219-150-75) / 500 mL in 1 BAG (65219-150-00) · 65219-150-75
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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