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    NDC 71335-0376-01 FENTANYL 12 ug/h Details

    FENTANYL 12 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 71335-0376
    Product ID 71335-0376_3a6cec6b-25c1-4e82-a9df-849511de3926
    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 12
    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 71335-0376-01 (71335037601)

    NDC Package Code 71335-0376-1
    Billing NDC 71335037601
    Package 1 h in 1 BOTTLE (71335-0376-1)
    Marketing Start Date 2017-05-31
    NDC Exclude Flag N
    Pricing Information N/A