Nadolol - 0781-1181-92 - (Nadolol)

Alphabetical Index


Drug Information of Nadolol

Product NDC: 0781-1181
Proprietary Name: Nadolol
Non Proprietary Name: Nadolol
Active Ingredient(s): 20    mg/1 & nbsp;   Nadolol
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Nadolol

Product NDC: 0781-1181
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074501
Marketing Category: ANDA
Start Marketing Date: 20081001

Package Information of Nadolol

Package NDC: 0781-1181-92
Package Description: 90 TABLET in 1 BOTTLE (0781-1181-92)

NDC Information of Nadolol

NDC Code 0781-1181-92
Proprietary Name Nadolol
Package Description 90 TABLET in 1 BOTTLE (0781-1181-92)
Product NDC 0781-1181
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nadolol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20081001
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name NADOLOL
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Nadolol


General Information