Label: ACD-A- antiocoagulant citrate dextrose solution, formula a solution

  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: New Drug Application

Drug Label Information

Updated June 4, 2012

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  • WARNINGS

    Do Not Use Unless Solution is Clear and Seal is Intact

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  • HOW SUPPLIED

    Sterile, Non-pyrogenic

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  • PACKAGE/LABEL PRINCIPAL DISPLAY PANEL
  • INGREDIENTS AND APPEARANCE
    ACD-A 
    antiocoagulant citrate dextrose solution, formula a solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0942-9005
    Route of Administration INTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    DEXTROSE MONOHYDRATE (UNII: LX22YL083G) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK) DEXTROSE MONOHYDRATE 2.45 g  in 100 mL
    SODIUM CITRATE (UNII: 1Q73Q2JULR) (ANHYDROUS CITRIC ACID - UNII:XF417D3PSL) SODIUM CITRATE 2.2 g  in 100 mL
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) (ANHYDROUS CITRIC ACID - UNII:XF417D3PSL) ANHYDROUS CITRIC ACID 730 mg  in 100 mL
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0942-9005-01 1000 mL in 1 BAG
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    NDA BN160918 10/24/2012
    Labeler - Fenwal Inc. (794519020)
    Registrant - Fenwal Inc. (794519020)
    Establishment
    Name Address ID/FEI Business Operations
    Fenwal International, Inc 091164590 MANUFACTURE(0942-9005)
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