Search by Drug Name or NDC

    NDC 00942-9201-01 Anticoagulant Citrate Phosphate Dextrose (CPD) Blood-Pack Units in PL 146 Plastic 105; 893; 78; 921 mg/35mL; mg/35mL; mg/35mL; mg/35mL Details

    Anticoagulant Citrate Phosphate Dextrose (CPD) Blood-Pack Units in PL 146 Plastic 105; 893; 78; 921 mg/35mL; mg/35mL; mg/35mL; mg/35mL

    Anticoagulant Citrate Phosphate Dextrose (CPD) Blood-Pack Units in PL 146 Plastic is a INTRAVENOUS SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Fenwal, Inc.. The primary component is ANHYDROUS CITRIC ACID; DEXTROSE MONOHYDRATE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE; TRISODIUM CITRATE DIHYDRATE.

    Product Information

    NDC 00942-9201
    Product ID 0942-9201_1ee1e424-2028-4b58-b554-883d2e359c28
    Associated GPIs
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    Proprietary Name Anticoagulant Citrate Phosphate Dextrose (CPD) Blood-Pack Units in PL 146 Plastic
    Proprietary Name Suffix n/a
    Non-Proprietary Name Anticoagulant Citrate Phosphate Dextrose (CPD) Solution
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form SOLUTION
    Route INTRAVENOUS
    Active Ingredient Strength 105; 893; 78; 921
    Active Ingredient Units mg/35mL; mg/35mL; mg/35mL; mg/35mL
    Substance Name ANHYDROUS CITRIC ACID; DEXTROSE MONOHYDRATE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE; TRISODIUM CITRATE DIHYDRATE
    Labeler Name Fenwal, Inc.
    Pharmaceutical Class Acidifying Activity [MoA], Acidifying Activity [MoA], Anti-coagulant [EPC], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Calculi Dissolution Agent [EPC], Decreased Coagulation F
    DEA Schedule n/a
    Marketing Category NDA
    Application Number BN170401
    Listing Certified Through 2024-12-31

    Package

    NDC 00942-9201-01 (00942920101)

    NDC Package Code 0942-9201-01
    Billing NDC 00942920101
    Package 35 mL in 1 BAG (0942-9201-01)
    Marketing Start Date 2007-03-01
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL d55cb701-9664-4931-8754-1a8cae68da06 Details

    Revised: 11/2022