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LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE - 21695-831-90 - (LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE)

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Drug Information of LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE

Product NDC: 21695-831
Proprietary Name: LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE
Non Proprietary Name: LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE
Active Ingredient(s): 25; 100    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: 21695-831
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078385
Marketing Category: ANDA
Start Marketing Date: 20101004

Package Information of LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE

Package NDC: 21695-831-90
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (21695-831-90)

NDC Information of LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE

NDC Code 21695-831-90
Proprietary Name LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (21695-831-90)
Product NDC 21695-831
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 20101004
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM
Strength Number 25; 100
Strength Unit mg/1; mg/1
Pharmaceutical Classes Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient],Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]

Complete Information of LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE


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