Atenolol - 53808-0207-1 - (Atenolol)

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Drug Information of Atenolol

Product NDC: 53808-0207
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: 53808-0207
Labeler Name: State of Florida DOH Central Pharmacy
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076900
Marketing Category: ANDA
Start Marketing Date: 20090701

Package Information of Atenolol

Package NDC: 53808-0207-1
Package Description: 30 TABLET in 1 BLISTER PACK (53808-0207-1)

NDC Information of Atenolol

NDC Code 53808-0207-1
Proprietary Name Atenolol
Package Description 30 TABLET in 1 BLISTER PACK (53808-0207-1)
Product NDC 53808-0207
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Atenolol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090701
Marketing Category Name ANDA
Labeler Name State of Florida DOH Central Pharmacy
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