PredniSONE - 54868-0908-3 - (PredniSONE)

Alphabetical Index


Drug Information of PredniSONE

Product NDC: 54868-0908
Proprietary Name: PredniSONE
Non Proprietary Name: PredniSONE
Active Ingredient(s): 50    mg/1 & nbsp;   PredniSONE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of PredniSONE

Product NDC: 54868-0908
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA084283
Marketing Category: ANDA
Start Marketing Date: 20091210

Package Information of PredniSONE

Package NDC: 54868-0908-3
Package Description: 50 TABLET in 1 BOTTLE (54868-0908-3)

NDC Information of PredniSONE

NDC Code 54868-0908-3
Proprietary Name PredniSONE
Package Description 50 TABLET in 1 BOTTLE (54868-0908-3)
Product NDC 54868-0908
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PredniSONE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091210
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name PREDNISONE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of PredniSONE


General Information