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Losartan Potassium - 0591-3745-19 - (Losartan Potassium)

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Drug Information of Losartan Potassium

Product NDC: 0591-3745
Proprietary Name: Losartan Potassium
Non Proprietary Name: Losartan Potassium
Active Ingredient(s): 25    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: 0591-3745
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: 0591-3745-19
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-3745-19)

NDC Information of Losartan Potassium

NDC Code 0591-3745-19
Proprietary Name Losartan Potassium
Package Description 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-3745-19)
Product NDC 0591-3745
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 25
Strength Unit mg/1
Pharmaceutical Classes Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]

Complete Information of Losartan Potassium


General Information