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    NDC 68788-7660-09 PRAVASTATIN SODIUM 80 mg/1 Details

    PRAVASTATIN SODIUM 80 mg/1

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

    Product Information

    NDC 68788-7660
    Product ID 68788-7660_5de54449-f40b-4ffc-b2df-e06bd674f4bd
    Associated GPIs 39400065100360
    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 80
    Active Ingredient Units mg/1
    Substance Name PRAVASTATIN SODIUM
    Labeler Name Preferred Pharmaceuticals Inc..
    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 68788-7660-09 (68788766009)

    NDC Package Code 68788-7660-9
    Billing NDC 68788766009
    Package 90 TABLET in 1 BOTTLE (68788-7660-9)
    Marketing Start Date 2022-09-27
    NDC Exclude Flag N
    Pricing Information N/A