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Losartan Potassium and Hydrochlorothiazide - 51079-757-20 - (losartan potassium and hydrochlorothiazide)

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Drug Information of Losartan Potassium and Hydrochlorothiazide

Product NDC: 51079-757
Proprietary Name: Losartan Potassium and Hydrochlorothiazide
Non Proprietary Name: losartan potassium and hydrochlorothiazide
Active Ingredient(s): 12.5; 50    mg/1; mg/1 & nbsp;   losartan potassium and hydrochlorothiazide
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Losartan Potassium and Hydrochlorothiazide

Product NDC: 51079-757
Labeler Name: UDL Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091652
Marketing Category: ANDA
Start Marketing Date: 20111006

Package Information of Losartan Potassium and Hydrochlorothiazide

Package NDC: 51079-757-20
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-757-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-757-01)

NDC Information of Losartan Potassium and Hydrochlorothiazide

NDC Code 51079-757-20
Proprietary Name Losartan Potassium and Hydrochlorothiazide
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-757-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-757-01)
Product NDC 51079-757
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name losartan potassium and hydrochlorothiazide
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20111006
Marketing Category Name ANDA
Labeler Name UDL Laboratories, Inc.
Substance Name HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM
Strength Number 12.5; 50
Strength Unit mg/1; mg/1
Pharmaceutical Classes Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]

Complete Information of Losartan Potassium and Hydrochlorothiazide


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