Atenolol - 43063-297-90 - (Atenolol)

Alphabetical Index


Drug Information of Atenolol

Product NDC: 43063-297
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: 43063-297
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074052
Marketing Category: ANDA
Start Marketing Date: 19920501

Package Information of Atenolol

Package NDC: 43063-297-90
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC (43063-297-90)

NDC Information of Atenolol

NDC Code 43063-297-90
Proprietary Name Atenolol
Package Description 90 TABLET in 1 BOTTLE, PLASTIC (43063-297-90)
Product NDC 43063-297
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 PD-Rx Pharmaceuticals, Inc.
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