Prednisone - 52125-366-02 - (Prednisone)

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Drug Information of Prednisone

Product NDC: 52125-366
Proprietary Name: Prednisone
Non Proprietary Name: Prednisone
Active Ingredient(s): 5    mg/1 & nbsp;   Prednisone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Prednisone

Product NDC: 52125-366
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040256
Marketing Category: ANDA
Start Marketing Date: 20130705

Package Information of Prednisone

Package NDC: 52125-366-02
Package Description: 30 TABLET in 1 BLISTER PACK (52125-366-02)

NDC Information of Prednisone

NDC Code 52125-366-02
Proprietary Name Prednisone
Package Description 30 TABLET in 1 BLISTER PACK (52125-366-02)
Product NDC 52125-366
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Prednisone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130705
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name PREDNISONE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Prednisone


General Information