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    NDC 68382-0071-10 pravastatin sodium 20 mg/1 Details

    pravastatin sodium 20 mg/1

    pravastatin sodium is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Zydus Pharmaceuticals USA Inc.. The primary component is PRAVASTATIN SODIUM.

    Product Information

    NDC 68382-0071
    Product ID 68382-071_12014495-c66a-407e-aa7b-5c58596230ce
    Associated GPIs 39400065100330
    GCN Sequence Number 016367
    GCN Sequence Number Description pravastatin sodium TABLET 20 MG ORAL
    HIC3 M4D
    HIC3 Description ANTIHYPERLIPIDEMIC-HMGCOA REDUCTASE INHIB(STATINS)
    GCN 48672
    HICL Sequence Number 006227
    HICL Sequence Number Description PRAVASTATIN SODIUM
    Brand/Generic Generic
    Proprietary Name pravastatin sodium
    Proprietary Name Suffix n/a
    Non-Proprietary Name pravastatin sodium
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 20
    Active Ingredient Units mg/1
    Substance Name PRAVASTATIN SODIUM
    Labeler Name Zydus Pharmaceuticals USA Inc.
    Pharmaceutical Class HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA077751
    Listing Certified Through 2024-12-31

    Package

    NDC 68382-0071-10 (68382007110)

    NDC Package Code 68382-071-10
    Billing NDC 68382007110
    Package 1000 TABLET in 1 BOTTLE (68382-071-10)
    Marketing Start Date 2010-03-30
    NDC Exclude Flag N
    Pricing Information N/A