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Anticoagulant Sodium Citrate - 62646-798-60 - (Sodium Citrate)

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Drug Information of Anticoagulant Sodium Citrate

Product NDC: 62646-798
Proprietary Name: Anticoagulant Sodium Citrate
Non Proprietary Name: Sodium Citrate
Active Ingredient(s): 10    g/250mL & nbsp;   Sodium Citrate
Administration Route(s): INTRAVENOUS
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Anticoagulant Sodium Citrate

Product NDC: 62646-798
Labeler Name: Medsep Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA760305
Marketing Category: NDA
Start Marketing Date: 20110415

Package Information of Anticoagulant Sodium Citrate

Package NDC: 62646-798-60
Package Description: 250 mL in 1 BAG (62646-798-60)

NDC Information of Anticoagulant Sodium Citrate

NDC Code 62646-798-60
Proprietary Name Anticoagulant Sodium Citrate
Package Description 250 mL in 1 BAG (62646-798-60)
Product NDC 62646-798
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sodium Citrate
Dosage Form Name SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20110415
Marketing Category Name NDA
Labeler Name Medsep Corporation
Substance Name SODIUM CITRATE
Strength Number 10
Strength Unit g/250mL
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 Sodium Citrate


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