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losartan potassium - 0781-5701-31 - (losartan potassium)

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Drug Information of losartan potassium

Product NDC: 0781-5701
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: 0781-5701
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077424
Marketing Category: ANDA
Start Marketing Date: 20101006

Package Information of losartan potassium

Package NDC: 0781-5701-31
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (0781-5701-31)

NDC Information of losartan potassium

NDC Code 0781-5701-31
Proprietary Name losartan potassium
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (0781-5701-31)
Product NDC 0781-5701
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name losartan potassium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20101006
Marketing Category Name ANDA
Labeler Name Sandoz Inc
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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