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    NDC 71335-1224-01 FENTANYL 50 ug/h Details

    FENTANYL 50 ug/h

    FENTANYL is a TRANSDERMAL PATCH, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is FENTANYL.

    Product Information

    NDC 71335-1224
    Product ID 71335-1224_077e4213-375f-40f2-8588-b5a711f5839b
    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 FENTANYL
    Proprietary Name Suffix n/a
    Non-Proprietary Name FENTANYL
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form PATCH, EXTENDED RELEASE
    Route TRANSDERMAL
    Active Ingredient Strength 50
    Active Ingredient Units ug/h
    Substance Name FENTANYL
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class Full Opioid Agonists [MoA], Opioid Agonist [EPC]
    DEA Schedule CII
    Marketing Category ANDA
    Application Number ANDA077449
    Listing Certified Through 2023-12-31

    Package

    NDC 71335-1224-01 (71335122401)

    NDC Package Code 71335-1224-1
    Billing NDC 71335122401
    Package 1 POUCH in 1 CASE (71335-1224-1) / 1 PATCH in 1 POUCH / 72 h in 1 PATCH
    Marketing Start Date 2018-01-10
    NDC Exclude Flag N
    Pricing Information N/A