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    NDC 24555-0015-03 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 Correct Rx Pharmacy Services, Inc.. The primary component is AMOXICILLIN.

    Product Information

    NDC 24555-0015
    Product ID 24555-0015_0c7d1406-7c8c-ef90-e063-6394a90ad8e5
    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 Correct Rx Pharmacy Services, Inc.
    Pharmaceutical Class Penicillin-class Antibacterial [EPC], Penicillins [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA065256
    Listing Certified Through 2025-12-31

    Package

    NDC 24555-0015-03 (24555001503)

    NDC Package Code 24555-0015-3
    Billing NDC 24555001503
    Package 30 TABLET, FILM COATED in 1 BLISTER PACK (24555-0015-3)
    Marketing Start Date 2024-01-01
    NDC Exclude Flag N
    Pricing Information N/A