DELFLEX - 49230-200-31 - (Dextrose Monohydrate, Sodium Chloride, Calcium Chloride, Magnesium Chloride, Sodium Lactate)

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Drug Information of DELFLEX

Product NDC: 49230-200
Proprietary Name: DELFLEX
Non Proprietary Name: Dextrose Monohydrate, Sodium Chloride, Calcium Chloride, Magnesium Chloride, Sodium Lactate
Active Ingredient(s): 25.7; 2.5; 5.08; 538; 409    mg/100mL; g/100mL; mg/100mL; mg/100mL; mg/100mL & nbsp;   Dextrose Monohydrate, Sodium Chloride, Calcium Chloride, Magnesium Chloride, Sodium Lactate
Administration Route(s): INTRAPERITONEAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of DELFLEX

Product NDC: 49230-200
Labeler Name: Fresenius Medical Care North America
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018883
Marketing Category: NDA
Start Marketing Date: 19841130

Package Information of DELFLEX

Package NDC: 49230-200-31
Package Description: 3000 mL in 1 BAG (49230-200-31)

NDC Information of DELFLEX

NDC Code 49230-200-31
Proprietary Name DELFLEX
Package Description 3000 mL in 1 BAG (49230-200-31)
Product NDC 49230-200
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dextrose Monohydrate, Sodium Chloride, Calcium Chloride, Magnesium Chloride, Sodium Lactate
Dosage Form Name SOLUTION
Route Name INTRAPERITONEAL
Start Marketing Date 19841130
Marketing Category Name NDA
Labeler Name Fresenius Medical Care North America
Substance Name CALCIUM CHLORIDE; DEXTROSE MONOHYDRATE; MAGNESIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE
Strength Number 25.7; 2.5; 5.08; 538; 409
Strength Unit mg/100mL; g/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]

Complete Information of DELFLEX


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