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    NDC 69367-0190-50 Zoledronic Acid 4 mg/5mL Details

    Zoledronic Acid 4 mg/5mL

    Zoledronic Acid is a INTRAVENOUS INJECTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Westminster Pharmaceuticals, LLC. The primary component is ZOLEDRONIC ACID.

    Product Information

    NDC 69367-0190
    Product ID 69367-190_d8c7e44e-b472-4c33-bfd7-1eb9d18b4a0f
    Associated GPIs
    GCN Sequence Number 051991
    GCN Sequence Number Description zoledronic acid VIAL 4 MG/5 ML INTRAVEN
    HIC3 P4L
    HIC3 Description BONE RESORPTION INHIBITORS
    GCN 19476
    HICL Sequence Number 021845
    HICL Sequence Number Description ZOLEDRONIC ACID
    Brand/Generic Generic
    Proprietary Name Zoledronic Acid
    Proprietary Name Suffix n/a
    Non-Proprietary Name Zoledronic Acid
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION
    Route INTRAVENOUS
    Active Ingredient Strength 4
    Active Ingredient Units mg/5mL
    Substance Name ZOLEDRONIC ACID
    Labeler Name Westminster Pharmaceuticals, LLC
    Pharmaceutical Class Bisphosphonate [EPC], Diphosphonates [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA202923
    Listing Certified Through 2024-12-31

    Package

    NDC 69367-0190-50 (69367019050)

    NDC Package Code 69367-190-50
    Billing NDC 69367019050
    Package 1 VIAL in 1 CARTON (69367-190-50) / 5 mL in 1 VIAL
    Marketing Start Date 2023-02-02
    NDC Exclude Flag N
    Pricing Information N/A