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    NDC 17856-0759-03 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 ATLANTIC BIOLOGICALS CORP.. The primary component is PREDNISOLONE SODIUM PHOSPHATE.

    Product Information

    NDC 17856-0759
    Product ID 17856-0759_8cae7975-b84d-42b2-abe0-242804fc68d0
    Associated GPIs 22100040202020
    GCN Sequence Number 047282
    GCN Sequence Number Description prednisolone sodium phosphate SOLUTION 15 MG/5 ML ORAL
    HIC3 P5A
    HIC3 Description GLUCOCORTICOIDS
    GCN 33806
    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 15
    Active Ingredient Units mg/5mL
    Substance Name PREDNISOLONE SODIUM PHOSPHATE
    Labeler Name ATLANTIC BIOLOGICALS CORP.
    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 17856-0759-03 (17856075903)

    NDC Package Code 17856-0759-3
    Billing NDC 17856075903
    Package 48 SYRINGE in 1 BOX, UNIT-DOSE (17856-0759-3) / 5 mL in 1 SYRINGE
    Marketing Start Date 2023-12-12
    NDC Exclude Flag N
    Pricing Information N/A