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    NDC 63187-0029-15 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 Proficient Rx LP. The primary component is AMOXICILLIN.

    Product Information

    NDC 63187-0029
    Product ID 63187-029_e61645ee-b492-46b5-bb37-8df0e39e20d8
    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 250
    Active Ingredient Units mg/5mL
    Substance Name AMOXICILLIN
    Labeler Name Proficient Rx LP
    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 63187-0029-15 (63187002915)

    NDC Package Code 63187-029-15
    Billing NDC 63187002915
    Package 150 mL in 1 BOTTLE (63187-029-15)
    Marketing Start Date 2014-05-01
    NDC Exclude Flag N
    Pricing Information N/A