59651-491 : Prednisolone 5 mg Oral Tablet


NDC: 59651-491
Labeler: Aurobindo Pharma Limited
Product Type: Human Prescription Drug
Drug Name:  Prednisolone
Dosage Form: Oral Tablet
Application #: ANDA215673
Rev. Date: 


NDC Package Codes:

  • 59651-491-01: 100 TABLET IN 1 BOTTLE (59651‑491‑01)
  • 59651-491-50: 50 TABLET IN 1 BOTTLE (59651‑491‑50)

Active Ingredients:

  • Prednisolone

Dosage Strength:

  • 5 mg

Pharmaceutical Classes:

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

Related Products:

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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.