Atenolol - 0615-3544-39 - (Atenolol)

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Drug Information of Atenolol

Product NDC: 0615-3544
Proprietary Name: Atenolol
Non Proprietary Name: Atenolol
Active Ingredient(s): 25    mg/1 & nbsp;   Atenolol
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Atenolol

Product NDC: 0615-3544
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074052
Marketing Category: ANDA
Start Marketing Date: 19920501

Package Information of Atenolol

Package NDC: 0615-3544-39
Package Description: 30 TABLET in 1 BLISTER PACK (0615-3544-39)

NDC Information of Atenolol

NDC Code 0615-3544-39
Proprietary Name Atenolol
Package Description 30 TABLET in 1 BLISTER PACK (0615-3544-39)
Product NDC 0615-3544
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Atenolol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19920501
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
Substance Name ATENOLOL
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Atenolol


General Information