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    NDC 42799-0813-01 Prednisolone Sodium Phosphate 20 mg/5mL Details

    Prednisolone Sodium Phosphate 20 mg/5mL

    Prednisolone Sodium Phosphate is a ORAL SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Edenbridge Pharmaceuticals LLC.. The primary component is PREDNISOLONE SODIUM PHOSPHATE.

    Product Information

    NDC 42799-0813
    Product ID 42799-813_073536da-16a0-4c78-b4d4-95a1e3ad00d6
    Associated GPIs 22100040202060
    GCN Sequence Number 064528
    GCN Sequence Number Description prednisolone sodium phosphate SOLUTION 20 MG/5 ML ORAL
    HIC3 P5A
    HIC3 Description GLUCOCORTICOIDS
    GCN 14565
    HICL Sequence Number 002871
    HICL Sequence Number Description PREDNISOLONE SODIUM PHOSPHATE
    Brand/Generic Generic
    Proprietary Name Prednisolone Sodium Phosphate
    Proprietary Name Suffix n/a
    Non-Proprietary Name Prednisolone Sodium Phosphate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form SOLUTION
    Route ORAL
    Active Ingredient Strength 20
    Active Ingredient Units mg/5mL
    Substance Name PREDNISOLONE SODIUM PHOSPHATE
    Labeler Name Edenbridge Pharmaceuticals LLC.
    Pharmaceutical Class Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA203559
    Listing Certified Through 2024-12-31

    Package

    NDC 42799-0813-01 (42799081301)

    NDC Package Code 42799-813-01
    Billing NDC 42799081301
    Package 237 mL in 1 BOTTLE, PLASTIC (42799-813-01)
    Marketing Start Date 2011-11-11
    NDC Exclude Flag N
    Pricing Information N/A