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Losortan Potassium - 68382-136-06 - (Losartan Potassium)

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Drug Information of Losortan Potassium

Product NDC: 68382-136
Proprietary Name: Losortan 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 Losortan Potassium

Product NDC: 68382-136
Labeler Name: Zydus Pharmaceuticals (USA) Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078243
Marketing Category: ANDA
Start Marketing Date: 20101004

Package Information of Losortan Potassium

Package NDC: 68382-136-06
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (68382-136-06)

NDC Information of Losortan Potassium

NDC Code 68382-136-06
Proprietary Name Losortan Potassium
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (68382-136-06)
Product NDC 68382-136
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Losartan Potassium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20101004
Marketing Category Name ANDA
Labeler Name Zydus Pharmaceuticals (USA) 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 Losortan Potassium


General Information