PredniSONE - 0615-6516-39 - (PredniSONE)

Alphabetical Index


Drug Information of PredniSONE

Product NDC: 0615-6516
Proprietary Name: PredniSONE
Non Proprietary Name: PredniSONE
Active Ingredient(s): 1    mg/1 & nbsp;   PredniSONE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of PredniSONE

Product NDC: 0615-6516
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA087800
Marketing Category: ANDA
Start Marketing Date: 19820422

Package Information of PredniSONE

Package NDC: 0615-6516-39
Package Description: 30 TABLET in 1 BLISTER PACK (0615-6516-39)

NDC Information of PredniSONE

NDC Code 0615-6516-39
Proprietary Name PredniSONE
Package Description 30 TABLET in 1 BLISTER PACK (0615-6516-39)
Product NDC 0615-6516
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PredniSONE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19820422
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
Substance Name PREDNISONE
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of PredniSONE


General Information