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    NDC 69263-0822-01 Beta 1 Kit Details

    Beta 1 Kit

    Beta 1 Kit is a INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR KIT in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Oaklock, LLC. The primary component is .

    Product Information

    NDC 69263-0822
    Product ID 69263-822_0c575686-2b73-89b9-e063-6294a90a812a
    Associated GPIs 22109902106430
    GCN Sequence Number 074731
    GCN Sequence Number Description betamethasone acetate,sod phos KIT 6 MG/ML INJECTION
    HIC3 P5A
    HIC3 Description GLUCOCORTICOIDS
    GCN 39468
    HICL Sequence Number 002881
    HICL Sequence Number Description BETAMETHASONE ACETATE/BETAMETHASONE SODIUM PHOSPHATE
    Brand/Generic Brand
    Proprietary Name Beta 1 Kit
    Proprietary Name Suffix n/a
    Non-Proprietary Name Betamethasone Sodium Phosphate, Betamethasone Acetate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form KIT
    Route INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR
    Active Ingredient Strength n/a
    Active Ingredient Units n/a
    Substance Name n/a
    Labeler Name Oaklock, LLC
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA090747
    Listing Certified Through 2024-12-31

    Package

    NDC 69263-0822-01 (69263082201)

    NDC Package Code 69263-822-01
    Billing NDC 69263082201
    Package 1 KIT in 1 CARTON (69263-822-01) * 1 VIAL, MULTI-DOSE in 1 CARTON (0517-0720-01) / 5 mL in 1 VIAL, MULTI-DOSE
    Marketing Start Date 2015-08-25
    NDC Exclude Flag N
    Pricing Information N/A