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LISINOPRIL AND HYDROCHLOROTHIAZIDE - 54868-4637-1 - (LISINOPRIL AND HYDROCHLOROTHIAZIDE)

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Drug Information of LISINOPRIL AND HYDROCHLOROTHIAZIDE

Product NDC: 54868-4637
Proprietary Name: LISINOPRIL AND HYDROCHLOROTHIAZIDE
Non Proprietary Name: LISINOPRIL AND HYDROCHLOROTHIAZIDE
Active Ingredient(s): 12.5; 20    mg/1; mg/1 & nbsp;   LISINOPRIL AND HYDROCHLOROTHIAZIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of LISINOPRIL AND HYDROCHLOROTHIAZIDE

Product NDC: 54868-4637
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076007
Marketing Category: ANDA
Start Marketing Date: 20090623

Package Information of LISINOPRIL AND HYDROCHLOROTHIAZIDE

Package NDC: 54868-4637-1
Package Description: 100 TABLET in 1 BOTTLE (54868-4637-1)

NDC Information of LISINOPRIL AND HYDROCHLOROTHIAZIDE

NDC Code 54868-4637-1
Proprietary Name LISINOPRIL AND HYDROCHLOROTHIAZIDE
Package Description 100 TABLET in 1 BOTTLE (54868-4637-1)
Product NDC 54868-4637
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name LISINOPRIL AND HYDROCHLOROTHIAZIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090623
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name HYDROCHLOROTHIAZIDE; LISINOPRIL
Strength Number 12.5; 20
Strength Unit mg/1; mg/1
Pharmaceutical Classes Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]

Complete Information of LISINOPRIL AND HYDROCHLOROTHIAZIDE


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