Prednisone - 10544-509-12 - (Prednisone)

Alphabetical Index


Drug Information of Prednisone

Product NDC: 10544-509
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: 10544-509
Labeler Name: Blenheim Pharmacal, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA083677
Marketing Category: ANDA
Start Marketing Date: 20100317

Package Information of Prednisone

Package NDC: 10544-509-12
Package Description: 12 TABLET in 1 BOTTLE (10544-509-12)

NDC Information of Prednisone

NDC Code 10544-509-12
Proprietary Name Prednisone
Package Description 12 TABLET in 1 BOTTLE (10544-509-12)
Product NDC 10544-509
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Prednisone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100317
Marketing Category Name ANDA
Labeler Name Blenheim Pharmacal, Inc.
Substance Name PREDNISONE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Prednisone


General Information