FDA
Potassium Chloride 20MEQ in Dextrose 5% and Sodium Chloride 0.3% in Plastic Container
Composition
- Active ingredients
- DEXTROSE 5GM/100ML; POTASSIUM CHLORIDE 298MG/100ML; SODIUM CHLORIDE 300MG/100ML
Official product information
Drugs@FDA lists the approved labels, letters and reviews for application NDA018876.
Prognia shows this product information for reference and learning. It is not treatment advice and can lag behind the official text. Always check the current product information and local protocols before prescribing.
At a glance
- Brand name
- Potassium Chloride 20MEQ in Dextrose 5% and Sodium Chloride 0.3% in Plastic Container
- Active substance
- dextrose
- Route
- Injection
- Dosage form
- Injectable
- Applicant
- Icu Medical Inc
- Status
- Discontinued
- FDA approval
- 17 Jan 1986
- Application
- NDA018876-008