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    NDC 68788-7290-03 Budesonide 0.25 mg/2mL Details

    Budesonide 0.25 mg/2mL

    Budesonide is a ORAL INHALANT in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is BUDESONIDE.

    Product Information

    NDC 68788-7290
    Product ID 68788-7290_f7d85dbe-2901-4a02-b09e-5a3ac66e9884
    Associated GPIs 44400015001830
    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 Budesonide
    Proprietary Name Suffix Inhalation Suspension
    Non-Proprietary Name Budesonide
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INHALANT
    Route ORAL
    Active Ingredient Strength 0.25
    Active Ingredient Units mg/2mL
    Substance Name BUDESONIDE
    Labeler Name Preferred Pharmaceuticals Inc.
    Pharmaceutical Class Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA205710
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-7290-03 (68788729003)

    NDC Package Code 68788-7290-3
    Billing NDC 68788729003
    Package 6 POUCH in 1 CARTON (68788-7290-3) / 5 AMPULE in 1 POUCH / 2 mL in 1 AMPULE
    Marketing Start Date 2019-01-21
    NDC Exclude Flag N
    Pricing Information N/A