PredniSONE - 55154-4946-0 - (PredniSONE)

Alphabetical Index


Drug Information of PredniSONE

Product NDC: 55154-4946
Proprietary Name: PredniSONE
Non Proprietary Name: PredniSONE
Active Ingredient(s): 20    mg/1 & nbsp;   PredniSONE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of PredniSONE

Product NDC: 55154-4946
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA087342
Marketing Category: ANDA
Start Marketing Date: 20030213

Package Information of PredniSONE

Package NDC: 55154-4946-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-4946-0) > 1 TABLET in 1 BLISTER PACK

NDC Information of PredniSONE

NDC Code 55154-4946-0
Proprietary Name PredniSONE
Package Description 10 BLISTER PACK in 1 BAG (55154-4946-0) > 1 TABLET in 1 BLISTER PACK
Product NDC 55154-4946
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PredniSONE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20030213
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name PREDNISONE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of PredniSONE


General Information