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    NDC 71335-1022-04 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 Bryant Ranch Prepack. The primary component is PRAVASTATIN SODIUM.

    Product Information

    NDC 71335-1022
    Product ID 71335-1022_04a466f1-6e78-4e52-a88d-524e0574aa1f
    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 Bryant Ranch Prepack
    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 71335-1022-04 (71335102204)

    NDC Package Code 71335-1022-4
    Billing NDC 71335102204
    Package 60 TABLET in 1 BOTTLE (71335-1022-4)
    Marketing Start Date 2021-12-20
    NDC Exclude Flag N
    Pricing Information N/A