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    NDC 68788-7673-03 Rosuvastatin 10 mg/1 Details

    Rosuvastatin 10 mg/1

    Rosuvastatin is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals, Inc.. The primary component is ROSUVASTATIN CALCIUM.

    Product Information

    NDC 68788-7673
    Product ID 68788-7673_83353bc1-a915-40b2-8269-1fc2526d99d2
    Associated GPIs 39400060100310
    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 Rosuvastatin
    Proprietary Name Suffix n/a
    Non-Proprietary Name Rosuvastatin
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 10
    Active Ingredient Units mg/1
    Substance Name ROSUVASTATIN CALCIUM
    Labeler Name Preferred Pharmaceuticals, Inc.
    Pharmaceutical Class HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA207616
    Listing Certified Through 2023-12-31

    Package

    NDC 68788-7673-03 (68788767303)

    NDC Package Code 68788-7673-3
    Billing NDC 68788767303
    Package 30 TABLET, FILM COATED in 1 BOTTLE (68788-7673-3)
    Marketing Start Date 2020-02-28
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL b1ad774f-ab04-4193-8c4f-596ae90882c1 Details

    Revised: 10/2022