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    NDC 60505-6129-06 Budesonide 32 ug/1 Details

    Budesonide 32 ug/1

    Budesonide is a NASAL SPRAY, METERED in the HUMAN OTC DRUG category. It is labeled and distributed by Apotex Corp.. The primary component is BUDESONIDE.

    Product Information

    NDC 60505-6129
    Product ID 60505-6129_0a582c6f-407e-6fea-bdf9-250a06409532
    Associated GPIs 42200015001810
    GCN Sequence Number 075590
    GCN Sequence Number Description budesonide SPRAY/PUMP 32 MCG NASAL
    HIC3 Q7P
    HIC3 Description NASAL ANTI-INFLAMMATORY STEROIDS
    GCN 40708
    HICL Sequence Number 006545
    HICL Sequence Number Description BUDESONIDE
    Brand/Generic Generic
    Proprietary Name Budesonide
    Proprietary Name Suffix n/a
    Non-Proprietary Name Budesonide
    Product Type HUMAN OTC DRUG
    Dosage Form SPRAY, METERED
    Route NASAL
    Active Ingredient Strength 32
    Active Ingredient Units ug/1
    Substance Name BUDESONIDE
    Labeler Name Apotex Corp.
    Pharmaceutical Class Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA078949
    Listing Certified Through 2024-12-31

    Package

    NDC 60505-6129-06 (60505612906)

    NDC Package Code 60505-6129-6
    Billing NDC 60505612906
    Package 2 BOTTLE, SPRAY in 1 CARTON (60505-6129-6) / 120 SPRAY, METERED in 1 BOTTLE, SPRAY
    Marketing Start Date 2016-04-19
    NDC Exclude Flag N
    Pricing Information N/A