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    NDC 42571-0162-44 AMOXICILLIN AND CLAVULANATE POTASSIUM 875; 125 mg/1; mg/1 Details

    AMOXICILLIN AND CLAVULANATE POTASSIUM 875; 125 mg/1; mg/1

    AMOXICILLIN AND CLAVULANATE POTASSIUM is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Micro Labs Limited. The primary component is AMOXICILLIN; CLAVULANATE POTASSIUM.

    Product Information

    NDC 42571-0162
    Product ID 42571-162_0b5d12f0-f60d-a002-e063-6394a90a0d80
    Associated GPIs 01990002200340
    GCN Sequence Number 024668
    GCN Sequence Number Description amoxicillin/potassium clav TABLET 875-125 MG ORAL
    HIC3 W1A
    HIC3 Description PENICILLIN ANTIBIOTICS
    GCN 67076
    HICL Sequence Number 003962
    HICL Sequence Number Description AMOXICILLIN/POTASSIUM CLAVULANATE
    Brand/Generic Generic
    Proprietary Name AMOXICILLIN AND CLAVULANATE POTASSIUM
    Proprietary Name Suffix n/a
    Non-Proprietary Name Amoxicillin and Clavulanate Potassium
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 875; 125
    Active Ingredient Units mg/1; mg/1
    Substance Name AMOXICILLIN; CLAVULANATE POTASSIUM
    Labeler Name Micro Labs Limited
    Pharmaceutical Class Penicillin-class Antibacterial [EPC], Penicillins [CS], beta Lactamase Inhibitor [EPC], beta Lactamase Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA204755
    Listing Certified Through 2024-12-31

    Package

    NDC 42571-0162-44 (42571016244)

    NDC Package Code 42571-162-44
    Billing NDC 42571016244
    Package 4 BLISTER PACK in 1 CARTON (42571-162-44) / 4 TABLET, FILM COATED in 1 BLISTER PACK (42571-162-43)
    Marketing Start Date 2017-03-01
    NDC Exclude Flag N
    Pricing Information N/A