Search by Drug Name or NDC

    NDC 71335-1663-02 Raloxifene Hydrochloride 60 mg/1 Details

    Raloxifene Hydrochloride 60 mg/1

    Raloxifene Hydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is RALOXIFENE HYDROCHLORIDE.

    Product Information

    NDC 71335-1663
    Product ID 71335-1663_7b4e97f4-da7c-4231-831b-3e5defd469cc
    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 Raloxifene Hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Raloxifene
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 60
    Active Ingredient Units mg/1
    Substance Name RALOXIFENE HYDROCHLORIDE
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class Estrogen Agonist/Antagonist [EPC], Selective Estrogen Receptor Modulators [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA090842
    Listing Certified Through 2022-12-31

    Package

    NDC 71335-1663-02 (71335166302)

    NDC Package Code 71335-1663-2
    Billing NDC 71335166302
    Package 30 TABLET in 1 BOTTLE (71335-1663-2)
    Marketing Start Date 2020-07-15
    NDC Exclude Flag N
    Pricing Information N/A