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    NDC 51660-0723-11 Levonorgestrel 1.5 mg/1 Details

    Levonorgestrel 1.5 mg/1

    Levonorgestrel is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by Ohm Laboratories Inc.. The primary component is LEVONORGESTREL.

    Product Information

    NDC 51660-0723
    Product ID 51660-723_c82a6cf9-b461-411a-8ded-b33917bbdd51
    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 Levonorgestrel
    Proprietary Name Suffix n/a
    Non-Proprietary Name Levonorgestrel
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 1.5
    Active Ingredient Units mg/1
    Substance Name LEVONORGESTREL
    Labeler Name Ohm Laboratories Inc.
    Pharmaceutical Class Inhibit Ovum Fertilization [PE], Progesterone Congeners [CS], Progesterone Congeners [CS], Progestin [EPC], Progestin-containing Intrauterine Device [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA202635
    Listing Certified Through 2024-12-31

    Package

    NDC 51660-0723-11 (51660072311)

    NDC Package Code 51660-723-11
    Billing NDC 51660072311
    Package 1 BLISTER PACK in 1 CARTON (51660-723-11) / 1 TABLET in 1 BLISTER PACK
    Marketing Start Date 2017-11-01
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 5c509934-8c11-4d7f-8506-5971c37cfc22 Details

    Revised: 12/2020