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Losartan Potassium - 63739-513-10 - (Losartan Potassium)

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Drug Information of Losartan Potassium

Product NDC: 63739-513
Proprietary Name: Losartan Potassium
Non Proprietary Name: Losartan Potassium
Active Ingredient(s): 25    mg/1 & nbsp;   Losartan Potassium
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Losartan Potassium

Product NDC: 63739-513
Labeler Name: McKesson Packaging Services a business unit of McKesson Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090382
Marketing Category: ANDA
Start Marketing Date: 20110601

Package Information of Losartan Potassium

Package NDC: 63739-513-10
Package Description: 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-513-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Losartan Potassium

NDC Code 63739-513-10
Proprietary Name Losartan Potassium
Package Description 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-513-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 63739-513
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Losartan Potassium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110601
Marketing Category Name ANDA
Labeler Name McKesson Packaging Services a business unit of McKesson Corporation
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 Losartan Potassium


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