Orapred Odt

Active Ingredient(s): Prednisolone Sodium Phosphate
FDA Approved: * June 1, 2006
Pharm Company: * BIOMARIN
Category: Steroids

* This drug may consist of multiple approval dates, manufacturers, or distributors. If applicable, they would be listed below under "NDC Database Records".



Orapred Odt Overview

Prednisolone is a steroid medication used to treat certain types of allergies, inflammatory conditions, autoimmune disorders, and cancers.[1][2] Some of these conditions include adrenocortical insufficiency, high blood calcium, rheumatoid arthritis, dermatitis, eye inflammation, asthma, and multiple sclerosis.[2] It is used by mouth, injection into a vein, as a skin cream, and as eye drops.[3] Side effects with short term use inc...

Read more Orapred Odt Details
Details May Include Instructions, Side Effects, Interactions, Etc. Drug monograph is from Wikipedia. All text is available under the terms of the GFDL (GNU Free Documentation License). Source: en.wikipedia.org/wiki/Prednisolone

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Possible Dosages for this and Related Drugs:

Prednisolone Sodium Phosphate
  • Injection: 20mg/ml, 25mg/ml, 50mg/ml, eq 20mg phosphate/ml
  • Liquid: 15mg/5ml
  • Ointment: eq 0.25% phosphate
  • Solution: 0.125%, 1%, 15mg/5ml, 5mg/5ml, 6.7mg/5ml
  • Suspension: 0.12%, 0.125%, 1%, 15mg/5ml, 5mg/5ml
  • Suspension/drops: 0.12%, 0.125%, 0.13%, 1%
  • Syrup: 15mg/5ml, 5mg/5ml
  • Tablet: 1mg, 2.5mg, 5mg
  • Tablet, Orally Disintegrating: 10mg, 15mg, 30mg
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

NDC Database Records for Orapred Odt: (3 results)

Sorted by National Drug Code
  • 59212-700 Orapred 10 mg/1 Oral Tablet, Orally Disintegrating by Concordia Pharmaceuticals Inc.
  • 59212-701 Orapred 15 mg/1 Oral Tablet, Orally Disintegrating by Concordia Pharmaceuticals Inc.
  • 59212-702 Orapred 30 mg/1 Oral Tablet, Orally Disintegrating by Concordia Pharmaceuticals Inc.

Other drugs which contain Prednisolone Sodium Phosphate or a similar ingredient: (11 results)

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