66993-844 : Prednisolone Sodium Phosphate 10 mg Oral Tablet, Orally Disintegrating


NDC: 66993-844
Labeler: Prasco Laboratories
Product Type: Human Prescription Drug
Drug Name: Prednisolone Sodium Phosphate Odt
Dosage Form: Oral Tablet, Orally Disintegrating
Application #: NDA021959
Rev. Date: 


Appearance:


Markings: ORA;10
Shapes:  Round
Colors:  White
Size (mm): 6
Segments: * 1

* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines.

NDC Package Codes:

  • 66993-844-35: 2 BLISTER PACK IN 1 CARTON (66993‑844‑35) > 6 TABLET, ORALLY DISINTEGRATING IN 1 BLISTER PACK (66993‑844‑51)
  • 66993-844-62: 8 BLISTER PACK IN 1 CARTON (66993‑844‑62) > 6 TABLET, ORALLY DISINTEGRATING IN 1 BLISTER PACK

Active Ingredients:

  • Prednisolone Sodium Phosphate

Dosage Strength:

  • 10 mg

Inactive Ingredients:

  • Citric Acid Monohydrate
  • Silicon Dioxide
  • Crospovidone
  • Hypromelloses
  • Magnesium Stearate
  • Mannitol
  • Cellulose, Microcrystalline
  • Sodium Bicarbonate
  • Sucralose
  • Sucrose
  • Methacrylic Acid - Methyl Methacrylate Copolymer (1:1)

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 66993-845 Prednisolone Sodium Phosphate 15 mg Oral Tablet, Orally Disintegrating by Prasco Laboratories

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.