Prednisone - 55289-352-15 - (Prednisone)

Alphabetical Index


Drug Information of Prednisone

Product NDC: 55289-352
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: 55289-352
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040392
Marketing Category: ANDA
Start Marketing Date: 20030212

Package Information of Prednisone

Package NDC: 55289-352-15
Package Description: 15 TABLET in 1 BOTTLE, PLASTIC (55289-352-15)

NDC Information of Prednisone

NDC Code 55289-352-15
Proprietary Name Prednisone
Package Description 15 TABLET in 1 BOTTLE, PLASTIC (55289-352-15)
Product NDC 55289-352
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Prednisone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20030212
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name PREDNISONE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Prednisone


General Information