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    NDC 50090-0822-02 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 A-S Medication Solutions. The primary component is AMOXICILLIN; CLAVULANATE POTASSIUM.

    Product Information

    NDC 50090-0822
    Product ID 50090-0822_0486c03e-39bd-4328-90c3-b84929648749
    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 A-S Medication Solutions
    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 ANDA091568
    Listing Certified Through 2024-12-31

    Package

    NDC 50090-0822-02 (50090082202)

    NDC Package Code 50090-0822-2
    Billing NDC 50090082202
    Package 14 TABLET, FILM COATED in 1 BOTTLE (50090-0822-2)
    Marketing Start Date 2014-11-28
    NDC Exclude Flag N
    Pricing Information N/A