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Losortan Potassium - 55154-2089-0 - (Losartan Potassium)

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Drug Information of Losortan Potassium

Product NDC: 55154-2089
Proprietary Name: Losortan Potassium
Non Proprietary Name: Losartan Potassium
Active Ingredient(s): 50    mg/1 & nbsp;   Losartan Potassium
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Losortan Potassium

Product NDC: 55154-2089
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078243
Marketing Category: ANDA
Start Marketing Date: 20101014

Package Information of Losortan Potassium

Package NDC: 55154-2089-0
Package Description: 1 BLISTER PACK in 1 BAG (55154-2089-0) > 10 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Losortan Potassium

NDC Code 55154-2089-0
Proprietary Name Losortan Potassium
Package Description 1 BLISTER PACK in 1 BAG (55154-2089-0) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 55154-2089
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Losartan Potassium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20101014
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name LOSARTAN POTASSIUM
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]

Complete Information of Losortan Potassium


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