Home > National Drug Code (NDC) > Lisinopril with Hydrochlorothiazide

Lisinopril with Hydrochlorothiazide - 67544-276-80 - (Lisinopril and Hydrochlorothiazide)

Alphabetical Index


Drug Information of Lisinopril with Hydrochlorothiazide

Product NDC: 67544-276
Proprietary Name: Lisinopril with 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 with Hydrochlorothiazide

Product NDC: 67544-276
Labeler Name: Aphena Pharma Solutions - Tennessee, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076265
Marketing Category: ANDA
Start Marketing Date: 20020708

Package Information of Lisinopril with Hydrochlorothiazide

Package NDC: 67544-276-80
Package Description: 180 TABLET in 1 BOTTLE, PLASTIC (67544-276-80)

NDC Information of Lisinopril with Hydrochlorothiazide

NDC Code 67544-276-80
Proprietary Name Lisinopril with Hydrochlorothiazide
Package Description 180 TABLET in 1 BOTTLE, PLASTIC (67544-276-80)
Product NDC 67544-276
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lisinopril and Hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20020708
Marketing Category Name ANDA
Labeler Name Aphena Pharma Solutions - Tennessee, LLC
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 with Hydrochlorothiazide


General Information