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    NDC 68180-0487-03 PRAVASTATIN SODIUM 40 mg/1 Details

    PRAVASTATIN SODIUM 40 mg/1

    PRAVASTATIN SODIUM is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Lupin Pharmaceuticals, Inc.. The primary component is PRAVASTATIN SODIUM.

    Product Information

    NDC 68180-0487
    Product ID 68180-487_a173dd76-57cb-4066-a51f-26adfb79e861
    Associated GPIs 39400065100340
    GCN Sequence Number 020741
    GCN Sequence Number Description pravastatin sodium TABLET 40 MG ORAL
    HIC3 M4D
    HIC3 Description ANTIHYPERLIPIDEMIC-HMGCOA REDUCTASE INHIB(STATINS)
    GCN 48673
    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 40
    Active Ingredient Units mg/1
    Substance Name PRAVASTATIN SODIUM
    Labeler Name Lupin Pharmaceuticals, Inc.
    Pharmaceutical Class HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA077917
    Listing Certified Through 2024-12-31

    Package

    NDC 68180-0487-03 (68180048703)

    NDC Package Code 68180-487-03
    Billing NDC 68180048703
    Package 1000 TABLET in 1 BOTTLE (68180-487-03)
    Marketing Start Date 2008-07-24
    NDC Exclude Flag N
    Pricing Information N/A