Prednisone - 21695-305-30 - (Prednisone)

Alphabetical Index


Drug Information of Prednisone

Product NDC: 21695-305
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: 21695-305
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA080292
Marketing Category: ANDA
Start Marketing Date: 19720522

Package Information of Prednisone

Package NDC: 21695-305-30
Package Description: 30 TABLET in 1 BOTTLE (21695-305-30)

NDC Information of Prednisone

NDC Code 21695-305-30
Proprietary Name Prednisone
Package Description 30 TABLET in 1 BOTTLE (21695-305-30)
Product NDC 21695-305
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Prednisone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19720522
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name PREDNISONE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Prednisone


General Information