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Losartan Potassium - 0591-3747-10 - (Losartan Potassium)

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Drug Information of Losartan Potassium

Product NDC: 0591-3747
Proprietary Name: Losartan Potassium
Non Proprietary Name: Losartan Potassium
Active Ingredient(s): 100    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: 0591-3747
Labeler Name: Watson Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091129
Marketing Category: ANDA
Start Marketing Date: 20110222

Package Information of Losartan Potassium

Package NDC: 0591-3747-10
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-3747-10)

NDC Information of Losartan Potassium

NDC Code 0591-3747-10
Proprietary Name Losartan Potassium
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-3747-10)
Product NDC 0591-3747
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Losartan Potassium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110222
Marketing Category Name ANDA
Labeler Name Watson Laboratories, Inc.
Substance Name LOSARTAN POTASSIUM
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]

Complete Information of Losartan Potassium


General Information