Prednisone - 52125-054-02 - (PREDNISONE)

Alphabetical Index


Drug Information of Prednisone

Product NDC: 52125-054
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: 52125-054
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA085161
Marketing Category: ANDA
Start Marketing Date: 20120912

Package Information of Prednisone

Package NDC: 52125-054-02
Package Description: 30 TABLET in 1 BLISTER PACK (52125-054-02)

NDC Information of Prednisone

NDC Code 52125-054-02
Proprietary Name Prednisone
Package Description 30 TABLET in 1 BLISTER PACK (52125-054-02)
Product NDC 52125-054
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PREDNISONE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120912
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name PREDNISONE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Prednisone


General Information