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    NDC 42291-0667-90 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 AvKARE. The primary component is PRAVASTATIN SODIUM.

    Product Information

    NDC 42291-0667
    Product ID 42291-667_052ace3f-bc7f-4936-e063-6394a90acd3b
    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 AvKARE
    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 42291-0667-90 (42291066790)

    NDC Package Code 42291-667-90
    Billing NDC 42291066790
    Package 90 TABLET in 1 BOTTLE (42291-667-90)
    Marketing Start Date 2014-06-30
    NDC Exclude Flag N
    Pricing Information N/A