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    NDC 68788-9948-01 Amoxicillin 250 mg/5mL Details

    Amoxicillin 250 mg/5mL

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

    Product Information

    NDC 68788-9948
    Product ID 68788-9948_357df73e-dbed-47e8-a0c7-5706f94cd063
    Associated GPIs 01200010101915
    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 250
    Active Ingredient Units mg/5mL
    Substance Name AMOXICILLIN
    Labeler Name Preferred Pharmaceuticals, Inc.
    Pharmaceutical Class Penicillin-class Antibacterial [EPC], Penicillins [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA065387
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-9948-01 (68788994801)

    NDC Package Code 68788-9948-1
    Billing NDC 68788994801
    Package 150 mL in 1 BOTTLE (68788-9948-1)
    Marketing Start Date 2012-01-12
    NDC Exclude Flag N
    Pricing Information N/A