Cardioplegic Solution
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Cardioplegic Solution
- Generic name
- POTASSIUM CHLORIDE, SODIUM CHLORIDE, CALCIUM CHLORIDE, AND MAGNESIUM CHLORIDE
- Manufacturer
- Fresenius Kabi, USA, LLC
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- eb360dc4-88d6-4b28-9b61-bc359e16bd22
- SPL ID
- 9c1af4dc-3653-49cb-baa5-e916369a4e0a
- Version
- 4
- Effective date
- 2022-05-27
- Source export date
- 2026-09-28
- Source partition
- 6
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:37:15
| Harmonized routes |
|---|
| INTRA-ARTERIAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application applno | ANDA | 214623 | derived:openfda.application_number |
| application number | ANDA214623 | openfda.application_number | |
| brand name | Cardioplegic Solution | openfda.brand_name | |
| generic name | POTASSIUM CHLORIDE, SODIUM CHLORIDE, CALCIUM CHLORIDE, AND MAGNESIUM CHLORIDE | openfda.generic_name | |
| manufacturer name | Fresenius Kabi, USA, LLC | openfda.manufacturer_name | |
| ndc | package | 65219-258-01 | openfda.package_ndc |
| ndc | package | 65219-258-10 | openfda.package_ndc |
| ndc | product | 65219-258 | openfda.product_ndc |
| ndc11 | package | 65219025810 | derived:openfda.package_ndc |
| ndc11 | package | 65219025801 | derived:openfda.package_ndc |
| spl id | 9c1af4dc-3653-49cb-baa5-e916369a4e0a | id | |
| spl set id | eb360dc4-88d6-4b28-9b61-bc359e16bd22 | set_id | |
| unii | 02F3473H9O | openfda.unii | |
| unii | 451W47IQ8X | openfda.unii | |
| unii | 660YQ98I10 | openfda.unii | |
| unii | M4I0D6VV5M | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
WARNINGS This solution should be used only by those trained to perform open heart surgery. This solution is intended only for use during cardiopulmonary bypass when the coronary circulation is isolated from the systemic circulation (See INDICATIONS AND USAGE ). Do not instill the solution into the coronary vasculature unless sodium bicarbonate has been added. If large volumes of cardioplegic solution are infused and allowed to return to the heart lung machine without any venting from the right heart, then plasma magnesium and potassium levels may rise. Development of severe hypotension and metabolic acidosis while on bypass has been reported when large volumes (8 to 10 liters) of solution are instilled and allowed to enter the pump and then the systemic circulation. Right heart venting is therefore recommended. The buffered solution with added sodium bicarbonate should be cooled to 4°C prior to administration and used within 24 hours of mixing.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
ADVERSE REACTIONS Intraoperative and perioperative potential hazards of open heart surgery include myocardial infarction, electrocardiographic abnormalities, and arrhythmias, including ventricular fibrillation. Spontaneous recovery after cardioplegic cardiac arrest may be delayed or absent when circulation is restored. Defibrillation by electric shock may be required to restore normal cardiac function. To report SUSPECTED ADVERSE REACTIONS, contact Fresenius Kabi USA, LLC at 1-800-551-7176 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.