Search by Drug Name or NDC

    NDC 68788-7708-02 Prednisolone Sodium Phosphate 15 mg/5mL Details

    Prednisolone Sodium Phosphate 15 mg/5mL

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

    Product Information

    NDC 68788-7708
    Product ID 68788-7708_ccc3562c-f23b-44e3-8230-6655c7051b15
    Associated GPIs 22100040202020
    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 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 15
    Active Ingredient Units mg/5mL
    Substance Name PREDNISOLONE SODIUM PHOSPHATE
    Labeler Name Preferred Pharmaceuticals, Inc.
    Pharmaceutical Class Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA076913
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-7708-02 (68788770802)

    NDC Package Code 68788-7708-2
    Billing NDC 68788770802
    Package 237 mL in 1 BOTTLE (68788-7708-2)
    Marketing Start Date 2020-06-01
    NDC Exclude Flag N
    Pricing Information N/A