CORGARD - 60793-802-01 - (nadolol)

Alphabetical Index


Drug Information of CORGARD

Product NDC: 60793-802
Proprietary Name: CORGARD
Non Proprietary Name: nadolol
Active Ingredient(s): 80    mg/1 & nbsp;   nadolol
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of CORGARD

Product NDC: 60793-802
Labeler Name: King Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018063
Marketing Category: NDA
Start Marketing Date: 19791210

Package Information of CORGARD

Package NDC: 60793-802-01
Package Description: 100 TABLET in 1 BOTTLE (60793-802-01)

NDC Information of CORGARD

NDC Code 60793-802-01
Proprietary Name CORGARD
Package Description 100 TABLET in 1 BOTTLE (60793-802-01)
Product NDC 60793-802
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name nadolol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19791210
Marketing Category Name NDA
Labeler Name King Pharmaceuticals, Inc.
Substance Name NADOLOL
Strength Number 80
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of CORGARD


General Information