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    NDC 00703-4636-01 Zanosar 100 mg/mL Details

    Zanosar 100 mg/mL

    Zanosar is a INTRAVENOUS POWDER, FOR SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Teva Parenteral Medicines, Inc.. The primary component is STREPTOZOCIN.

    Product Information

    NDC 00703-4636
    Product ID 0703-4636_086af066-2d97-4c11-9f8d-68eb4f7c29f3
    Associated GPIs 21102030002105
    GCN Sequence Number 008825
    GCN Sequence Number Description streptozocin VIAL 1 G INTRAVEN
    HIC3 V1D
    HIC3 Description ANTIBIOTIC ANTINEOPLASTICS
    GCN 38630
    HICL Sequence Number 003920
    HICL Sequence Number Description STREPTOZOCIN
    Brand/Generic Brand
    Proprietary Name Zanosar
    Proprietary Name Suffix n/a
    Non-Proprietary Name streptozocin
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form POWDER, FOR SOLUTION
    Route INTRAVENOUS
    Active Ingredient Strength 100
    Active Ingredient Units mg/mL
    Substance Name STREPTOZOCIN
    Labeler Name Teva Parenteral Medicines, Inc.
    Pharmaceutical Class Alkylating Activity [MoA], Alkylating Drug [EPC]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA050577
    Listing Certified Through 2024-12-31

    Package

    NDC 00703-4636-01 (00703463601)

    NDC Package Code 0703-4636-01
    Billing NDC 00703463601
    Package 10 mL in 1 VIAL (0703-4636-01)
    Marketing Start Date 2003-12-03
    NDC Exclude Flag N
    Pricing Information N/A