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LOSARTAN POTASSIUM - 42571-111-90 - (losartan potassium)

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Drug Information of LOSARTAN POTASSIUM

Product NDC: 42571-111
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, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of LOSARTAN POTASSIUM

Product NDC: 42571-111
Labeler Name: Micro Labs Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091541
Marketing Category: ANDA
Start Marketing Date: 20121206

Package Information of LOSARTAN POTASSIUM

Package NDC: 42571-111-90
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (42571-111-90)

NDC Information of LOSARTAN POTASSIUM

NDC Code 42571-111-90
Proprietary Name LOSARTAN POTASSIUM
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (42571-111-90)
Product NDC 42571-111
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name losartan potassium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20121206
Marketing Category Name ANDA
Labeler Name Micro Labs Limited
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


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