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Anticoagulant Citrate Dextrose A - 23731-6051-5 - (ANHYDROUS CITRIC ACID, DEXTROSE MONOHYDRATE, and TRISODIUM CITRATE DIHYDRATE)

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Drug Information of Anticoagulant Citrate Dextrose A

Product NDC: 23731-6051
Proprietary Name: Anticoagulant Citrate Dextrose A
Non Proprietary Name: ANHYDROUS CITRIC ACID, DEXTROSE MONOHYDRATE, and TRISODIUM CITRATE DIHYDRATE
Active Ingredient(s): 7.3; 24.5; 22    mg/mL; mg/mL; mg/mL & nbsp;   ANHYDROUS CITRIC ACID, DEXTROSE MONOHYDRATE, and TRISODIUM CITRATE DIHYDRATE
Administration Route(s): EXTRACORPOREAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Anticoagulant Citrate Dextrose A

Product NDC: 23731-6051
Labeler Name: Citra Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BN020037
Marketing Category: NDA
Start Marketing Date: 20030710

Package Information of Anticoagulant Citrate Dextrose A

Package NDC: 23731-6051-5
Package Description: 12 BOTTLE, GLASS in 1 BOX (23731-6051-5) > 50 mL in 1 BOTTLE, GLASS

NDC Information of Anticoagulant Citrate Dextrose A

NDC Code 23731-6051-5
Proprietary Name Anticoagulant Citrate Dextrose A
Package Description 12 BOTTLE, GLASS in 1 BOX (23731-6051-5) > 50 mL in 1 BOTTLE, GLASS
Product NDC 23731-6051
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ANHYDROUS CITRIC ACID, DEXTROSE MONOHYDRATE, and TRISODIUM CITRATE DIHYDRATE
Dosage Form Name SOLUTION
Route Name EXTRACORPOREAL
Start Marketing Date 20030710
Marketing Category Name NDA
Labeler Name Citra Labs
Substance Name ANHYDROUS CITRIC ACID; DEXTROSE MONOHYDRATE; TRISODIUM CITRATE DIHYDRATE
Strength Number 7.3; 24.5; 22
Strength Unit mg/mL; mg/mL; mg/mL
Pharmaceutical Classes Acidifying Activity [MoA],Calculi Dissolution Agent [EPC],Anti-coagulant [EPC],Decreased Coagulation Factor Activity [PE],Calcium Chelating Activity [MoA]

Complete Information of Anticoagulant Citrate Dextrose A


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