Cozaar - 49349-233-02 - (Cozaar)

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Drug Information of Cozaar

Product NDC: 49349-233
Proprietary Name: Cozaar
Non Proprietary Name: Cozaar
Active Ingredient(s): 25    mg/1 & nbsp;   Cozaar
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Cozaar

Product NDC: 49349-233
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020386
Marketing Category: NDA
Start Marketing Date: 20110519

Package Information of Cozaar

Package NDC: 49349-233-02
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (49349-233-02)

NDC Information of Cozaar

NDC Code 49349-233-02
Proprietary Name Cozaar
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (49349-233-02)
Product NDC 49349-233
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cozaar
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110519
Marketing Category Name NDA
Labeler Name REMEDYREPACK INC.
Substance Name LOSARTAN POTASSIUM
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]

Complete Information of Cozaar


General Information