NDC 0338-0341

Cardioplegic

Calcium Chloride, Magnesium Chloride, Potassium Chloride And Sodium Chloride

Cardioplegic is a Intra-arterial Solution in the Human Prescription Drug category. It is labeled and distributed by Baxter Healthcare Corporation. The primary component is Calcium Chloride; Magnesium Chloride; Potassium Chloride; Sodium Chloride.

Product ID0338-0341_10d0d308-0148-434e-930a-fd27a25e5389
NDC0338-0341
Product TypeHuman Prescription Drug
Proprietary NameCardioplegic
Generic NameCalcium Chloride, Magnesium Chloride, Potassium Chloride And Sodium Chloride
Dosage FormSolution
Route of AdministrationINTRA-ARTERIAL
Marketing Start Date2000-04-21
Marketing CategoryANDA / ANDA
Application NumberANDA075323
Labeler NameBaxter Healthcare Corporation
Substance NameCALCIUM CHLORIDE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE
Active Ingredient Strength18 mg/100mL; mg/100mL; mg/100mL; mg/100mL
Pharm ClassesBlood Coagulation Factor [EPC], Calcium [CS], Calculi Dissolution Agent [EPC], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 0338-0341-04

14 BAG in 1 CARTON (0338-0341-04) > 1000 mL in 1 BAG
Marketing Start Date2000-04-21
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0338-0341-04 [00338034104]

Cardioplegic SOLUTION
Marketing CategoryANDA
Application NumberANDA075323
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2000-04-21

Drug Details

Active Ingredients

IngredientStrength
CALCIUM CHLORIDE17.6 mg/100mL

OpenFDA Data

SPL SET ID:1fd50ce5-2799-4c26-81da-02cf0578dd9e
Manufacturer
UNII

Pharmacological Class

  • Blood Coagulation Factor [EPC]
  • Increased Coagulation Factor Activity [PE]
  • Calcium [CS]
  • Cations
  • Divalent [CS]
  • Calculi Dissolution Agent [EPC]
  • Magnesium Ion Exchange Activity [MoA]
  • Osmotic Laxative [EPC]
  • Osmotic Activity [MoA]
  • Inhibition Small Intestine Fluid/Electrolyte Absorption [PE]
  • Increased Large Intestinal Motility [PE]
  • Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
  • Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]
  • Potassium Compounds [CS]
  • Potassium Salt [EPC]
  • Osmotic Laxative [EPC]
  • Increased Large Intestinal Motility [PE]
  • Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]
  • Osmotic Activity [MoA]
  • Osmotic Laxative [EPC]
  • Increased Large Intestinal Motility [PE]
  • Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]
  • Osmotic Activity [MoA]

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