PredniSONE - 0054-0018-25 - (PredniSONE)

Alphabetical Index


Drug Information of PredniSONE

Product NDC: 0054-0018
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: 0054-0018
Labeler Name: Roxane Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA087342
Marketing Category: ANDA
Start Marketing Date: 20030213

Package Information of PredniSONE

Package NDC: 0054-0018-25
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (0054-0018-25)

NDC Information of PredniSONE

NDC Code 0054-0018-25
Proprietary Name PredniSONE
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (0054-0018-25)
Product NDC 0054-0018
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 Roxane Laboratories, Inc.
Substance Name PREDNISONE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of PredniSONE


General Information