Prednisone - 59746-172-06 - (Prednisone)

Alphabetical Index


Drug Information of Prednisone

Product NDC: 59746-172
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: 59746-172
Labeler Name: JUBILANT CADISTA PHARMACEUTICALS, INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040362
Marketing Category: ANDA
Start Marketing Date: 20010829

Package Information of Prednisone

Package NDC: 59746-172-06
Package Description: 100 TABLET in 1 BOTTLE (59746-172-06)

NDC Information of Prednisone

NDC Code 59746-172-06
Proprietary Name Prednisone
Package Description 100 TABLET in 1 BOTTLE (59746-172-06)
Product NDC 59746-172
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Prednisone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20010829
Marketing Category Name ANDA
Labeler Name JUBILANT CADISTA PHARMACEUTICALS, INC.
Substance Name PREDNISONE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Prednisone


General Information