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    NDC 69238-2026-07 Amlodipine 1 mg/mL Details

    Amlodipine 1 mg/mL

    Amlodipine is a ORAL SUSPENSION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Amneal Pharmaceuticals NY LLC. The primary component is AMLODIPINE BENZOATE.

    Product Information

    NDC 69238-2026
    Product ID 69238-2026_f18fa3f2-2d8f-499f-9708-3748fee89eb3
    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 Amlodipine
    Proprietary Name Suffix n/a
    Non-Proprietary Name Amlodipine
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form SUSPENSION
    Route ORAL
    Active Ingredient Strength 1
    Active Ingredient Units mg/mL
    Substance Name AMLODIPINE BENZOATE
    Labeler Name Amneal Pharmaceuticals NY LLC
    Pharmaceutical Class Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA215035
    Listing Certified Through 2024-12-31

    Package

    NDC 69238-2026-07 (69238202607)

    NDC Package Code 69238-2026-7
    Billing NDC 69238202607
    Package 1 BOTTLE in 1 CARTON (69238-2026-7) / 150 mL in 1 BOTTLE
    Marketing Start Date 2023-06-16
    NDC Exclude Flag N
    Pricing Information N/A