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    NDC 51655-0441-21 Metronidazole 500 mg/1 Details

    Metronidazole 500 mg/1

    Metronidazole is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Northwind Pharmaceuticals, LLC. The primary component is METRONIDAZOLE.

    Product Information

    NDC 51655-0441
    Product ID 51655-441_ff9730da-7770-1902-e053-6394a90a015d
    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 Metronidazole
    Proprietary Name Suffix n/a
    Non-Proprietary Name METRONIDAZOLE
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 500
    Active Ingredient Units mg/1
    Substance Name METRONIDAZOLE
    Labeler Name Northwind Pharmaceuticals, LLC
    Pharmaceutical Class Nitroimidazole Antimicrobial [EPC], Nitroimidazoles [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA205245
    Listing Certified Through 2024-12-31

    Package

    NDC 51655-0441-21 (51655044121)

    NDC Package Code 51655-441-21
    Billing NDC 51655044121
    Package 21 TABLET in 1 BOTTLE, PLASTIC (51655-441-21)
    Marketing Start Date 2022-11-30
    NDC Exclude Flag N
    Pricing Information N/A