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    NDC 51285-0128-70 Loestrin Details

    Loestrin

    Loestrin is a KIT in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Teva Women's Health LLC. The primary component is .

    Product Information

    NDC 51285-0128
    Product ID 51285-128_ac1ba264-f0d0-4aea-b392-66924639042b
    Associated GPIs 25990003610320
    GCN Sequence Number 003300
    GCN Sequence Number Description norethindrone-e.estradiol-iron TABLET 1.5-30(21) ORAL
    HIC3 G8A
    HIC3 Description CONTRACEPTIVES,ORAL
    GCN 68101
    HICL Sequence Number 001454
    HICL Sequence Number Description NORETHINDRONE ACETATE-ETHINYL ESTRADIOL/FERROUS FUMARATE
    Brand/Generic Brand
    Proprietary Name Loestrin
    Proprietary Name Suffix Fe 28 Day
    Non-Proprietary Name Norethindrone Acetate and Ethinyl Estradiol and Ferrous Fumarate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form KIT
    Route n/a
    Active Ingredient Strength n/a
    Active Ingredient Units n/a
    Substance Name n/a
    Labeler Name Teva Women's Health LLC
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA076064
    Listing Certified Through 2024-12-31

    Package

    NDC 51285-0128-70 (51285012870)

    NDC Package Code 51285-128-70
    Billing NDC 51285012870
    Package 5 POUCH in 1 CARTON (51285-128-70) / 1 BLISTER PACK in 1 POUCH / 1 KIT in 1 BLISTER PACK
    Marketing Start Date 2015-02-26
    NDC Exclude Flag N
    Pricing Information N/A