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Prednisolone - 58177-910-07 - (Prednisolone)

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Drug Information of Prednisolone

Product NDC: 58177-910
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: 58177-910
Labeler Name: ETHEX Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040364
Marketing Category: ANDA
Start Marketing Date: 20040510

Package Information of Prednisolone

Package NDC: 58177-910-07
Package Description: 480 mL in 1 BOTTLE (58177-910-07)

NDC Information of Prednisolone

NDC Code 58177-910-07
Proprietary Name Prednisolone
Package Description 480 mL in 1 BOTTLE (58177-910-07)
Product NDC 58177-910
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Prednisolone
Dosage Form Name SYRUP
Route Name ORAL
Start Marketing Date 20040510
Marketing Category Name ANDA
Labeler Name ETHEX Corporation
Substance Name PREDNISOLONE
Strength Number 15
Strength Unit mg/5mL
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Prednisolone


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