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Losartan Potassium - 13668-409-10 - (Losartan Potassium)

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Drug Information of Losartan Potassium

Product NDC: 13668-409
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: 13668-409
Labeler Name: Torrent Pharmaceuticals Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090467
Marketing Category: ANDA
Start Marketing Date: 20101006

Package Information of Losartan Potassium

Package NDC: 13668-409-10
Package Description: 1000 TABLET in 1 BOTTLE (13668-409-10)

NDC Information of Losartan Potassium

NDC Code 13668-409-10
Proprietary Name Losartan Potassium
Package Description 1000 TABLET in 1 BOTTLE (13668-409-10)
Product NDC 13668-409
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 Torrent Pharmaceuticals 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


General Information