COZAAR - 55289-238-30 - (losartan potassium)

Alphabetical Index


Drug Information of COZAAR

Product NDC: 55289-238
Proprietary Name: COZAAR
Non Proprietary Name: losartan potassium
Active Ingredient(s): 100    mg/1 & nbsp;   losartan potassium
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of COZAAR

Product NDC: 55289-238
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020386
Marketing Category: NDA
Start Marketing Date: 19950414

Package Information of COZAAR

Package NDC: 55289-238-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-238-30)

NDC Information of COZAAR

NDC Code 55289-238-30
Proprietary Name COZAAR
Package Description 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-238-30)
Product NDC 55289-238
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name losartan potassium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19950414
Marketing Category Name NDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name LOSARTAN POTASSIUM
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]

Complete Information of COZAAR


General Information