Atenolol - 49349-336-02 - (Atenolol)

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Drug Information of Atenolol

Product NDC: 49349-336
Proprietary Name: Atenolol
Non Proprietary Name: Atenolol
Active Ingredient(s): 100    mg/1 & nbsp;   Atenolol
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Atenolol

Product NDC: 49349-336
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077877
Marketing Category: ANDA
Start Marketing Date: 20110713

Package Information of Atenolol

Package NDC: 49349-336-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-336-02)

NDC Information of Atenolol

NDC Code 49349-336-02
Proprietary Name Atenolol
Package Description 30 TABLET in 1 BLISTER PACK (49349-336-02)
Product NDC 49349-336
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Atenolol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110713
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name ATENOLOL
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Atenolol


General Information