53014-250 : Pediapred 6.7 mg/5ml Oral Solution


NDC: 53014-250
Labeler: Ucb Manufacturing, Inc.
Product Type: Human Prescription Drug
Drug Name:  Pediapred
Dosage Form: Oral Solution
Application #: NDA019157
Rev. Date: 


NDC Package Codes:

  • 53014-250-01: 120 ML IN 1 BOTTLE (53014‑250‑01)

Active Ingredients:

  • Prednisolone Sodium Phosphate

Dosage Strength:

  • 6.7 mg/5mL

Pharmaceutical Classes:

  • Corticosteroid [EPC]
  • Corticosteroid Hormone Receptor Agonists [MoA]

Related Products:

Based on records with the same trade name.
  • 68791-100 Pediapred 5 mg/5ml Oral Solution by Royal Pharmaceuticals
  • 68791-104 Pediapred 5 mg/5ml Oral Solution by Royal Pharmaceuticals

NDC QR Code

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NDC 53014-250 QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.