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Losartan Potassium - 0093-7365-56 - (Losartan Potassium)

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Drug Information of Losartan Potassium

Product NDC: 0093-7365
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: 0093-7365
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076958
Marketing Category: ANDA
Start Marketing Date: 20100406

Package Information of Losartan Potassium

Package NDC: 0093-7365-56
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (0093-7365-56)

NDC Information of Losartan Potassium

NDC Code 0093-7365-56
Proprietary Name Losartan Potassium
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (0093-7365-56)
Product NDC 0093-7365
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Losartan Potassium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100406
Marketing Category Name ANDA
Labeler Name Teva 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 Losartan Potassium


General Information