PredniSONE - 49349-607-08 - (PredniSONE)

Alphabetical Index


Drug Information of PredniSONE

Product NDC: 49349-607
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: 49349-607
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA084283
Marketing Category: ANDA
Start Marketing Date: 20130703

Package Information of PredniSONE

Package NDC: 49349-607-08
Package Description: 10 TABLET in 1 VIAL (49349-607-08)

NDC Information of PredniSONE

NDC Code 49349-607-08
Proprietary Name PredniSONE
Package Description 10 TABLET in 1 VIAL (49349-607-08)
Product NDC 49349-607
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PredniSONE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130703
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name PREDNISONE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of PredniSONE


General Information