Nadolol - 54868-5295-1 - (nadolol)

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Drug Information of Nadolol

Product NDC: 54868-5295
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: 54868-5295
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074172
Marketing Category: ANDA
Start Marketing Date: 20050516

Package Information of Nadolol

Package NDC: 54868-5295-1
Package Description: 30 TABLET in 1 BOTTLE (54868-5295-1)

NDC Information of Nadolol

NDC Code 54868-5295-1
Proprietary Name Nadolol
Package Description 30 TABLET in 1 BOTTLE (54868-5295-1)
Product NDC 54868-5295
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name nadolol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20050516
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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