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Losartan Potassium and Hydrochlorothiazide - 54868-6110-0 - (Losartan Potassium and Hydrochlorothiazide)

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Drug Information of Losartan Potassium and Hydrochlorothiazide

Product NDC: 54868-6110
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: 54868-6110
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077157
Marketing Category: ANDA
Start Marketing Date: 20100419

Package Information of Losartan Potassium and Hydrochlorothiazide

Package NDC: 54868-6110-0
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (54868-6110-0)

NDC Information of Losartan Potassium and Hydrochlorothiazide

NDC Code 54868-6110-0
Proprietary Name Losartan Potassium and Hydrochlorothiazide
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (54868-6110-0)
Product NDC 54868-6110
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 20100419
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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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