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Lisinopril and Hydrochlorothiazide - 51079-697-40 - (lisinopril and hydrochlorothiazide)

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Drug Information of Lisinopril and Hydrochlorothiazide

Product NDC: 51079-697
Proprietary Name: Lisinopril and Hydrochlorothiazide
Non Proprietary Name: lisinopril and hydrochlorothiazide
Active Ingredient(s): 12.5; 10    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: 51079-697
Labeler Name: UDL Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076113
Marketing Category: ANDA
Start Marketing Date: 20100607

Package Information of Lisinopril and Hydrochlorothiazide

Package NDC: 51079-697-40
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (51079-697-40)

NDC Information of Lisinopril and Hydrochlorothiazide

NDC Code 51079-697-40
Proprietary Name Lisinopril and Hydrochlorothiazide
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (51079-697-40)
Product NDC 51079-697
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name lisinopril and hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100607
Marketing Category Name ANDA
Labeler Name UDL Laboratories, Inc.
Substance Name HYDROCHLOROTHIAZIDE; LISINOPRIL
Strength Number 12.5; 10
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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