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Cardioplegic
Cardioplegic - 0338-0341-04 - (Calcium Chloride, Magnesium Chloride, Potassium Chloride and Sodium Chloride)
Drug Information of Cardioplegic
| Product NDC: | 0338-0341 |
| Proprietary Name: | Cardioplegic |
| Non Proprietary Name: | Calcium Chloride, Magnesium Chloride, Potassium Chloride and Sodium Chloride |
| Active Ingredient(s): | 17.6; 325.3; 119.3; 643 mg/100mL; mg/100mL; mg/100mL; mg/100mL & nbsp; Calcium Chloride, Magnesium Chloride, Potassium Chloride and Sodium Chloride |
| Administration Route(s): | INTRA-ARTERIAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cardioplegic
| Product NDC: | 0338-0341 |
| Labeler Name: | Baxter Healthcare Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075323 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110826 |
Package Information of Cardioplegic
| Package NDC: | 0338-0341-04 |
| Package Description: | 1000 mL in 1 BAG (0338-0341-04) |
NDC Information of Cardioplegic
| NDC Code | 0338-0341-04 |
| Proprietary Name | Cardioplegic |
| Package Description | 1000 mL in 1 BAG (0338-0341-04) |
| Product NDC | 0338-0341 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Calcium Chloride, Magnesium Chloride, Potassium Chloride and Sodium Chloride |
| Dosage Form Name | SOLUTION |
| Route Name | INTRA-ARTERIAL |
| Start Marketing Date | 20110826 |
| Marketing Category Name | ANDA |
| Labeler Name | Baxter Healthcare Corporation |
| Substance Name | CALCIUM CHLORIDE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE |
| Strength Number | 17.6; 325.3; 119.3; 643 |
| Strength Unit | mg/100mL; mg/100mL; mg/100mL; mg/100mL |
| Pharmaceutical Classes | Blood Coagulation Factor [EPC],Increased Coagulation Factor Activity [PE],Calcium [Chemical/Ingredient],Cations, Divalent [Chemical/Ingredient],Calculi Dissolution Agent [EPC],Magnesium Ion Exchange Activity [MoA],Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |
