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    NDC 61919-0708-30 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 Direct_Rx. The primary component is PRAVASTATIN SODIUM.

    Product Information

    NDC 61919-0708
    Product ID 61919-708_0e994ad4-d03f-9670-e063-6294a90adad3
    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 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 2025-12-31

    Package

    NDC 61919-0708-30 (61919070830)

    NDC Package Code 61919-708-30
    Billing NDC 61919070830
    Package 30 TABLET in 1 BOTTLE (61919-708-30)
    Marketing Start Date 2019-01-15
    NDC Exclude Flag N
    Pricing Information N/A