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    NDC 68788-7720-09 levothyroxine sodium 137 ug/1 Details

    levothyroxine sodium 137 ug/1

    levothyroxine sodium is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals, Inc.. The primary component is LEVOTHYROXINE SODIUM.

    Product Information

    NDC 68788-7720
    Product ID 68788-7720_de2ca0fb-b87e-4a37-8c6e-c690242bd9b1
    Associated GPIs 28100010100327
    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 levothyroxine sodium
    Proprietary Name Suffix n/a
    Non-Proprietary Name levothyroxine sodium
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 137
    Active Ingredient Units ug/1
    Substance Name LEVOTHYROXINE SODIUM
    Labeler Name Preferred Pharmaceuticals, Inc.
    Pharmaceutical Class Thyroxine [CS], l-Thyroxine [EPC]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA021116
    Listing Certified Through 2023-12-31

    Package

    NDC 68788-7720-09 (68788772009)

    NDC Package Code 68788-7720-9
    Billing NDC 68788772009
    Package 90 TABLET in 1 BOTTLE (68788-7720-9)
    Marketing Start Date 2020-07-01
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL bafd075c-2681-49a5-a411-9815b3dea3b3 Details

    Revised: 7/2022