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    NDC 61919-0707-90 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 DIRECT RX. The primary component is PRAVASTATIN SODIUM.

    Product Information

    NDC 61919-0707
    Product ID 61919-707_ff97ce4a-765d-540b-e053-6394a90ae328
    Associated GPIs 39400065100320
    GCN Sequence Number 016366
    GCN Sequence Number Description pravastatin sodium TABLET 10 MG ORAL
    HIC3 M4D
    HIC3 Description ANTIHYPERLIPIDEMIC-HMGCOA REDUCTASE INHIB(STATINS)
    GCN 48671
    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 10
    Active Ingredient Units mg/1
    Substance Name PRAVASTATIN SODIUM
    Labeler Name DIRECT RX
    Pharmaceutical Class HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA207068
    Listing Certified Through 2024-12-31

    Package

    NDC 61919-0707-90 (61919070790)

    NDC Package Code 61919-707-90
    Billing NDC 61919070790
    Package 90 TABLET in 1 BOTTLE (61919-707-90)
    Marketing Start Date 2018-12-19
    NDC Exclude Flag N
    Pricing Information N/A