Prednisone - 63629-1587-1 - (Prednisone)

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Drug Information of Prednisone

Product NDC: 63629-1587
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: 63629-1587
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040392
Marketing Category: ANDA
Start Marketing Date: 20030212

Package Information of Prednisone

Package NDC: 63629-1587-1
Package Description: 20 TABLET in 1 BOTTLE (63629-1587-1)

NDC Information of Prednisone

NDC Code 63629-1587-1
Proprietary Name Prednisone
Package Description 20 TABLET in 1 BOTTLE (63629-1587-1)
Product NDC 63629-1587
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 Bryant Ranch Prepack
Substance Name PREDNISONE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Prednisone


General Information