Prednisone - 68387-241-15 - (PREDNISONE)

Alphabetical Index


Drug Information of Prednisone

Product NDC: 68387-241
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: 68387-241
Labeler Name: Keltman Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA083677
Marketing Category: ANDA
Start Marketing Date: 20080707

Package Information of Prednisone

Package NDC: 68387-241-15
Package Description: 15 TABLET in 1 BOTTLE, PLASTIC (68387-241-15)

NDC Information of Prednisone

NDC Code 68387-241-15
Proprietary Name Prednisone
Package Description 15 TABLET in 1 BOTTLE, PLASTIC (68387-241-15)
Product NDC 68387-241
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PREDNISONE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080707
Marketing Category Name ANDA
Labeler Name Keltman Pharmaceuticals Inc.
Substance Name PREDNISONE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Prednisone


General Information