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    NDC 61919-0135-20 AMOXIL 875 mg/1 Details

    AMOXIL 875 mg/1

    AMOXIL is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by DIRECT RX. The primary component is AMOXICILLIN.

    Product Information

    NDC 61919-0135
    Product ID 61919-135_f2026976-ae4b-a6ea-e053-2a95a90ae6ac
    Associated GPIs 01200010100315
    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 AMOXIL
    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 DIRECT RX
    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 61919-0135-20 (61919013520)

    NDC Package Code 61919-135-20
    Billing NDC 61919013520
    Package 20 TABLET, FILM COATED in 1 BOTTLE (61919-135-20)
    Marketing Start Date 2016-07-08
    NDC Exclude Flag N
    Pricing Information N/A