Prednisone - 35356-673-20 - (Prednisone)

Alphabetical Index


Drug Information of Prednisone

Product NDC: 35356-673
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: 35356-673
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA080292
Marketing Category: ANDA
Start Marketing Date: 19720522

Package Information of Prednisone

Package NDC: 35356-673-20
Package Description: 20 TABLET in 1 BOTTLE (35356-673-20)

NDC Information of Prednisone

NDC Code 35356-673-20
Proprietary Name Prednisone
Package Description 20 TABLET in 1 BOTTLE (35356-673-20)
Product NDC 35356-673
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 Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name PREDNISONE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Prednisone


General Information