PredniSONE - 54868-1183-1 - (PredniSONE)

Alphabetical Index


Drug Information of PredniSONE

Product NDC: 54868-1183
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: 54868-1183
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA087342
Marketing Category: ANDA
Start Marketing Date: 20030819

Package Information of PredniSONE

Package NDC: 54868-1183-1
Package Description: 15 TABLET in 1 BOTTLE (54868-1183-1)

NDC Information of PredniSONE

NDC Code 54868-1183-1
Proprietary Name PredniSONE
Package Description 15 TABLET in 1 BOTTLE (54868-1183-1)
Product NDC 54868-1183
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PredniSONE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20030819
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name PREDNISONE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of PredniSONE


General Information