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    NDC 70436-0211-80 iopamidol 408 mg/mL Details

    iopamidol 408 mg/mL

    iopamidol is a INTRAVASCULAR INJECTION, SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Slate Run Pharmaceuticals, LLC. The primary component is IOPAMIDOL.

    Product Information

    NDC 70436-0211
    Product ID 70436-211_0766fa73-6d2f-748f-e063-6294a90a5c7f
    Associated GPIs
    GCN Sequence Number 000433
    GCN Sequence Number Description iopamidol VIAL 200 MG/ML INJECTION
    HIC3 A6U
    HIC3 Description CARDIOVASCULAR DIAGNOSTICS-RADIOPAQUE
    GCN 10900
    HICL Sequence Number 000150
    HICL Sequence Number Description IOPAMIDOL
    Brand/Generic Generic
    Proprietary Name iopamidol
    Proprietary Name Suffix n/a
    Non-Proprietary Name iopamidol
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION, SOLUTION
    Route INTRAVASCULAR
    Active Ingredient Strength 408
    Active Ingredient Units mg/mL
    Substance Name IOPAMIDOL
    Labeler Name Slate Run Pharmaceuticals, LLC
    Pharmaceutical Class Radiographic Contrast Agent [EPC], X-Ray Contrast Activity [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA217134
    Listing Certified Through 2024-12-31

    Package

    NDC 70436-0211-80 (70436021180)

    NDC Package Code 70436-211-80
    Billing NDC 70436021180
    Package 1 VIAL, SINGLE-DOSE in 1 CARTON (70436-211-80) / 50 mL in 1 VIAL, SINGLE-DOSE (70436-211-37)
    Marketing Start Date 2023-09-27
    NDC Exclude Flag N
    Pricing Information N/A