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    NDC 70518-2505-00 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 REMEDYREPACK INC.. The primary component is PRAVASTATIN SODIUM.

    Product Information

    NDC 70518-2505
    Product ID 70518-2505_04281248-15a2-9f62-e063-6294a90a0a13
    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 40
    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 70518-2505-00 (70518250500)

    NDC Package Code 70518-2505-0
    Billing NDC 70518250500
    Package 30 TABLET in 1 BLISTER PACK (70518-2505-0)
    Marketing Start Date 2019-12-24
    NDC Exclude Flag N
    Pricing Information N/A