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LISINOPRIL AND HYDROCHLOROTHIAZIDE - 63629-3739-3 - (LISINOPRIL AND HYDROCHLOROTHIAZIDE)

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Drug Information of LISINOPRIL AND HYDROCHLOROTHIAZIDE

Product NDC: 63629-3739
Proprietary Name: LISINOPRIL AND HYDROCHLOROTHIAZIDE
Non Proprietary Name: LISINOPRIL AND HYDROCHLOROTHIAZIDE
Active Ingredient(s): 25; 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: 63629-3739
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077912
Marketing Category: ANDA
Start Marketing Date: 20061002

Package Information of LISINOPRIL AND HYDROCHLOROTHIAZIDE

Package NDC: 63629-3739-3
Package Description: 90 TABLET in 1 BOTTLE (63629-3739-3)

NDC Information of LISINOPRIL AND HYDROCHLOROTHIAZIDE

NDC Code 63629-3739-3
Proprietary Name LISINOPRIL AND HYDROCHLOROTHIAZIDE
Package Description 90 TABLET in 1 BOTTLE (63629-3739-3)
Product NDC 63629-3739
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name LISINOPRIL AND HYDROCHLOROTHIAZIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20061002
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name HYDROCHLOROTHIAZIDE; LISINOPRIL
Strength Number 25; 20
Strength Unit mg/1; mg/1
Pharmaceutical Classes Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient],Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]

Complete Information of LISINOPRIL AND HYDROCHLOROTHIAZIDE


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