Atenolol - 49999-104-30 - (Atenolol)

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Drug Information of Atenolol

Product NDC: 49999-104
Proprietary Name: Atenolol
Non Proprietary Name: Atenolol
Active Ingredient(s): 50    mg/1 & nbsp;   Atenolol
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Atenolol

Product NDC: 49999-104
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077877
Marketing Category: ANDA
Start Marketing Date: 20100524

Package Information of Atenolol

Package NDC: 49999-104-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (49999-104-30)

NDC Information of Atenolol

NDC Code 49999-104-30
Proprietary Name Atenolol
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (49999-104-30)
Product NDC 49999-104
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Atenolol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100524
Marketing Category Name ANDA
Labeler Name Lake Erie Medical DBA Quality Care Products LLC
Substance Name ATENOLOL
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Atenolol


General Information