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Lisinopril and Hydrochlorothiazide - 65862-044-30 - (Lisinopril and Hydrochlorothiazide)

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Drug Information of Lisinopril and Hydrochlorothiazide

Product NDC: 65862-044
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: 65862-044
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077606
Marketing Category: ANDA
Start Marketing Date: 20060314

Package Information of Lisinopril and Hydrochlorothiazide

Package NDC: 65862-044-30
Package Description: 30 TABLET in 1 BOTTLE (65862-044-30)

NDC Information of Lisinopril and Hydrochlorothiazide

NDC Code 65862-044-30
Proprietary Name Lisinopril and Hydrochlorothiazide
Package Description 30 TABLET in 1 BOTTLE (65862-044-30)
Product NDC 65862-044
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lisinopril and Hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20060314
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
Substance Name HYDROCHLOROTHIAZIDE; LISINOPRIL
Strength Number 12.5; 20
Strength Unit mg/1; mg/1
Pharmaceutical Classes Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]

Complete Information of Lisinopril and Hydrochlorothiazide


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