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    NDC 71205-0149-30 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 Proficient Rx LP. The primary component is PRAVASTATIN SODIUM.

    Product Information

    NDC 71205-0149
    Product ID 71205-149_5b6275ce-603e-4ccf-83dd-1104dbf5c83f
    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 Proficient Rx LP
    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 71205-0149-30 (71205014930)

    NDC Package Code 71205-149-30
    Billing NDC 71205014930
    Package 30 TABLET in 1 BOTTLE (71205-149-30)
    Marketing Start Date 2018-11-01
    NDC Exclude Flag N
    Pricing Information N/A