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Prednisolone - 54868-4749-0 - (prednisolone)

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Drug Information of Prednisolone

Product NDC: 54868-4749
Proprietary Name: Prednisolone
Non Proprietary Name: prednisolone
Active Ingredient(s): 15    mg/5mL & nbsp;   prednisolone
Administration Route(s): ORAL
Dosage Form(s): SYRUP
Coding System: National Drug Codes(NDC)

Labeler Information of Prednisolone

Product NDC: 54868-4749
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040323
Marketing Category: ANDA
Start Marketing Date: 20030228

Package Information of Prednisolone

Package NDC: 54868-4749-0
Package Description: 240 mL in 1 BOTTLE (54868-4749-0)

NDC Information of Prednisolone

NDC Code 54868-4749-0
Proprietary Name Prednisolone
Package Description 240 mL in 1 BOTTLE (54868-4749-0)
Product NDC 54868-4749
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name prednisolone
Dosage Form Name SYRUP
Route Name ORAL
Start Marketing Date 20030228
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name PREDNISOLONE
Strength Number 15
Strength Unit mg/5mL
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Prednisolone


General Information