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    NDC 68071-1760-01 Amoxicillin 125 mg/5mL Details

    Amoxicillin 125 mg/5mL

    Amoxicillin is a ORAL POWDER, FOR SUSPENSION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by NuCare Pharmaceuticals,Inc.. The primary component is AMOXICILLIN.

    Product Information

    NDC 68071-1760
    Product ID 68071-1760_d6ac8710-cad8-69af-e053-2a95a90ae476
    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 POWDER, FOR SUSPENSION
    Route ORAL
    Active Ingredient Strength 125
    Active Ingredient Units mg/5mL
    Substance Name AMOXICILLIN
    Labeler Name NuCare Pharmaceuticals,Inc.
    Pharmaceutical Class Penicillin-class Antibacterial [EPC], Penicillins [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA065322
    Listing Certified Through 2024-12-31

    Package

    NDC 68071-1760-01 (68071176001)

    NDC Package Code 68071-1760-1
    Billing NDC 68071176001
    Package 100 mL in 1 BOTTLE (68071-1760-1)
    Marketing Start Date 2017-12-04
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 5f8b3c58-ed9f-84a2-e053-2a91aa0ac8cf Details

    Revised: 1/2022