PredniSONE - 55289-330-10 - (PredniSONE)

Alphabetical Index


Drug Information of PredniSONE

Product NDC: 55289-330
Proprietary Name: PredniSONE
Non Proprietary Name: PredniSONE
Active Ingredient(s): 10    mg/1 & nbsp;   PredniSONE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of PredniSONE

Product NDC: 55289-330
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA084122
Marketing Category: ANDA
Start Marketing Date: 20030213

Package Information of PredniSONE

Package NDC: 55289-330-10
Package Description: 10 BOTTLE, PLASTIC in 1 BOTTLE, PLASTIC (55289-330-10) > 7 TABLET in 1 BOTTLE, PLASTIC (55289-330-07)

NDC Information of PredniSONE

NDC Code 55289-330-10
Proprietary Name PredniSONE
Package Description 10 BOTTLE, PLASTIC in 1 BOTTLE, PLASTIC (55289-330-10) > 7 TABLET in 1 BOTTLE, PLASTIC (55289-330-07)
Product NDC 55289-330
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 PD-Rx Pharmaceuticals, Inc.
Substance Name PREDNISONE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of PredniSONE


General Information