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    NDC 70518-2887-01 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 REMEDYREPACK INC.. The primary component is PRAVASTATIN SODIUM.

    Product Information

    NDC 70518-2887
    Product ID 70518-2887_04dbda97-f40f-846e-e063-6394a90afaf6
    Associated GPIs
    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 20
    Active Ingredient Units mg/1
    Substance Name PRAVASTATIN SODIUM
    Labeler Name REMEDYREPACK INC.
    Pharmaceutical Class HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA076056
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-2887-01 (70518288701)

    NDC Package Code 70518-2887-1
    Billing NDC 70518288701
    Package 90 TABLET in 1 BOTTLE, PLASTIC (70518-2887-1)
    Marketing Start Date 2022-09-16
    NDC Exclude Flag N
    Pricing Information N/A