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    NDC 70518-3234-00 Amoxicillin 500 mg/1 Details

    Amoxicillin 500 mg/1

    Amoxicillin is a ORAL CAPSULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is AMOXICILLIN.

    Product Information

    NDC 70518-3234
    Product ID 70518-3234_0670e41c-4b35-59d4-e063-6394a90a3fe1
    Associated GPIs 01200010100110
    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 Amoxicillin
    Proprietary Name Suffix n/a
    Non-Proprietary Name Amoxicillin
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form CAPSULE
    Route ORAL
    Active Ingredient Strength 500
    Active Ingredient Units mg/1
    Substance Name AMOXICILLIN
    Labeler Name REMEDYREPACK INC.
    Pharmaceutical Class Penicillin-class Antibacterial [EPC], Penicillins [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA061926
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-3234-00 (70518323400)

    NDC Package Code 70518-3234-0
    Billing NDC 70518323400
    Package 100 POUCH in 1 BOX (70518-3234-0) / 1 CAPSULE in 1 POUCH
    Marketing Start Date 2021-10-11
    NDC Exclude Flag N
    Pricing Information N/A