Prednisone - 0591-5442-05 - (Prednisone)

Alphabetical Index


Drug Information of Prednisone

Product NDC: 0591-5442
Proprietary Name: Prednisone
Non Proprietary Name: Prednisone
Active Ingredient(s): 10    mg/1 & nbsp;   Prednisone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Prednisone

Product NDC: 0591-5442
Labeler Name: Watson Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA085162
Marketing Category: ANDA
Start Marketing Date: 19871101

Package Information of Prednisone

Package NDC: 0591-5442-05
Package Description: 500 TABLET in 1 BOTTLE (0591-5442-05)

NDC Information of Prednisone

NDC Code 0591-5442-05
Proprietary Name Prednisone
Package Description 500 TABLET in 1 BOTTLE (0591-5442-05)
Product NDC 0591-5442
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Prednisone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19871101
Marketing Category Name ANDA
Labeler Name Watson Laboratories, Inc.
Substance Name PREDNISONE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Prednisone


General Information