Orapred - 59630-710-08 - (prednisolone sodium phosphate)

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Drug Information of Orapred

Product NDC: 59630-710
Proprietary Name: Orapred
Non Proprietary Name: prednisolone sodium phosphate
Active Ingredient(s): 15    mg/5mL & nbsp;   prednisolone sodium phosphate
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Orapred

Product NDC: 59630-710
Labeler Name: Shionogi Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075117
Marketing Category: ANDA
Start Marketing Date: 20001214

Package Information of Orapred

Package NDC: 59630-710-08
Package Description: 237 mL in 1 BOTTLE, GLASS (59630-710-08)

NDC Information of Orapred

NDC Code 59630-710-08
Proprietary Name Orapred
Package Description 237 mL in 1 BOTTLE, GLASS (59630-710-08)
Product NDC 59630-710
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name prednisolone sodium phosphate
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20001214
Marketing Category Name ANDA
Labeler Name Shionogi Inc.
Substance Name PREDNISOLONE SODIUM PHOSPHATE
Strength Number 15
Strength Unit mg/5mL
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Orapred


General Information