Orapred - 59630-700-48 - (prednisolone sodium phosphate)

Alphabetical Index


Drug Information of Orapred

Product NDC: 59630-700
Proprietary Name: Orapred
Non Proprietary Name: prednisolone sodium phosphate
Active Ingredient(s): 10    mg/1 & nbsp;   prednisolone sodium phosphate
Administration Route(s): ORAL
Dosage Form(s): TABLET, ORALLY DISINTEGRATING
Coding System: National Drug Codes(NDC)

Labeler Information of Orapred

Product NDC: 59630-700
Labeler Name: Shionogi Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021959
Marketing Category: NDA
Start Marketing Date: 20060601

Package Information of Orapred

Package NDC: 59630-700-48
Package Description: 8 BLISTER PACK in 1 CARTON (59630-700-48) > 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

NDC Information of Orapred

NDC Code 59630-700-48
Proprietary Name Orapred
Package Description 8 BLISTER PACK in 1 CARTON (59630-700-48) > 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
Product NDC 59630-700
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name prednisolone sodium phosphate
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20060601
Marketing Category Name NDA
Labeler Name Shionogi Inc.
Substance Name PREDNISOLONE SODIUM PHOSPHATE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Orapred


General Information