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    NDC 71335-1435-04 levothyroxine sodium 200 ug/1 Details

    levothyroxine sodium 200 ug/1

    levothyroxine sodium is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is LEVOTHYROXINE SODIUM.

    Product Information

    NDC 71335-1435
    Product ID 71335-1435_21e53fb4-01c2-4ee0-a9fe-09fb50e29917
    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 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 200
    Active Ingredient Units ug/1
    Substance Name LEVOTHYROXINE SODIUM
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class Thyroxine [CS], l-Thyroxine [EPC]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA021116
    Listing Certified Through 2024-12-31

    Package

    NDC 71335-1435-04 (71335143504)

    NDC Package Code 71335-1435-4
    Billing NDC 71335143504
    Package 60 TABLET in 1 BOTTLE (71335-1435-4)
    Marketing Start Date 2019-12-12
    NDC Exclude Flag N
    Pricing Information N/A