Search by Drug Name or NDC

    NDC 43063-0443-30 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 PD-Rx Pharmaceuticals, Inc.. The primary component is PRAVASTATIN SODIUM.

    Product Information

    NDC 43063-0443
    Product ID 43063-443_f578e291-886d-6322-e053-2995a90a9d50
    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 PD-Rx Pharmaceuticals, 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 43063-0443-30 (43063044330)

    NDC Package Code 43063-443-30
    Billing NDC 43063044330
    Package 30 TABLET in 1 BOTTLE, PLASTIC (43063-443-30)
    Marketing Start Date 2012-10-22
    NDC Exclude Flag N
    Pricing Information N/A