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Losartan Potassium - 35356-884-30 - (Losartan Potassium)

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Drug Information of Losartan Potassium

Product NDC: 35356-884
Proprietary Name: Losartan Potassium
Non Proprietary Name: Losartan Potassium
Active Ingredient(s): 50    mg/1 & nbsp;   Losartan Potassium
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Losartan Potassium

Product NDC: 35356-884
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090467
Marketing Category: ANDA
Start Marketing Date: 20101006

Package Information of Losartan Potassium

Package NDC: 35356-884-30
Package Description: 30 TABLET in 1 BOTTLE (35356-884-30)

NDC Information of Losartan Potassium

NDC Code 35356-884-30
Proprietary Name Losartan Potassium
Package Description 30 TABLET in 1 BOTTLE (35356-884-30)
Product NDC 35356-884
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Losartan Potassium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101006
Marketing Category Name ANDA
Labeler Name Lake Erie Medical DBA Quality Care Products LLC
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 Losartan Potassium


General Information