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    NDC 70934-0418-30 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 Denton Pharma, Inc. DBA Northwind Pharmaceuticals. The primary component is PRAVASTATIN SODIUM.

    Product Information

    NDC 70934-0418
    Product ID 70934-418_d813587e-5ec4-662f-e053-2a95a90ac27e
    Associated GPIs 39400065100330
    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 Denton Pharma, Inc. DBA Northwind Pharmaceuticals
    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 n/a

    Package

    NDC 70934-0418-30 (70934041830)

    NDC Package Code 70934-418-30
    Billing NDC 70934041830
    Package 30 TABLET in 1 BOTTLE, PLASTIC (70934-418-30)
    Marketing Start Date 2019-08-05
    NDC Exclude Flag N
    Pricing Information N/A
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