0527-5406 : Prednisolone 15 mg/5ml Oral Syrup


NDC: 0527-5406
Labeler: Lannett Company, Inc.
Product Type: Human Prescription Drug
Drug Name:  Prednisolone
Dosage Form: Oral Syrup
Application #: ANDA040775
Rev. Date: 


NDC Package Codes:

  • 0527-5406-68: 240 ML IN 1 BOTTLE (0527‑5406‑68)
  • 0527-5406-70: 480 ML IN 1 BOTTLE (0527‑5406‑70)

Active Ingredients:

  • Prednisolone

Dosage Strength:

  • 15 mg/5mL

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
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  • 50090-2522 Prednisolone 15 mg/5ml Oral Syrup by A-s Medication Solutions
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  • 50383-042 Prednisolone 15 mg/5ml Oral Solution by Hi-tech Pharmacal Co., Inc.
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  • 58177-910 Prednisolone 15 mg/5ml Oral Syrup by Ethex Corporation
  • 59651-491 Prednisolone 5 mg Oral Tablet by Aurobindo Pharma Limited
  • 60722-5011 Prednisolone 5 mg Oral Tablet by Zhejiang Xianju Pharmaceutical Co., Ltd.
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NDC 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.