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    NDC 35356-0921-30 Pravastatin Sodium 10 mg/1 Details

    Pravastatin Sodium 10 mg/1

    Pravastatin Sodium is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Lake Erie Medical DBA Quality Care Products LLC. The primary component is PRAVASTATIN SODIUM.

    Product Information

    NDC 35356-0921
    Product ID 35356-921_9bef500a-9612-442a-9ab9-1dc9da83b35b
    Associated GPIs 39400065100320
    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 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 10
    Active Ingredient Units mg/1
    Substance Name PRAVASTATIN SODIUM
    Labeler Name Lake Erie Medical DBA Quality Care Products LLC
    Pharmaceutical Class HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA076341
    Listing Certified Through 2024-12-31

    Package

    NDC 35356-0921-30 (35356092130)

    NDC Package Code 35356-921-30
    Billing NDC 35356092130
    Package 30 TABLET in 1 BOTTLE (35356-921-30)
    Marketing Start Date 2011-07-18
    NDC Exclude Flag N
    Pricing Information N/A