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    NDC 68788-7414-02 Amoxicillin 875 mg/1 Details

    Amoxicillin 875 mg/1

    Amoxicillin is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is AMOXICILLIN.

    Product Information

    NDC 68788-7414
    Product ID 68788-7414_5682f98b-22a7-4b4d-beb1-dd061850baa7
    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 Amoxicillin
    Proprietary Name Suffix n/a
    Non-Proprietary Name Amoxicillin
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 875
    Active Ingredient Units mg/1
    Substance Name AMOXICILLIN
    Labeler Name Preferred Pharmaceuticals Inc.
    Pharmaceutical Class Penicillin-class Antibacterial [EPC], Penicillins [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA065256
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-7414-02 (68788741402)

    NDC Package Code 68788-7414-2
    Billing NDC 68788741402
    Package 20 TABLET, FILM COATED in 1 BOTTLE (68788-7414-2)
    Marketing Start Date 2020-03-25
    NDC Exclude Flag N
    Pricing Information N/A