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Lisinopril with Hydrochlorothiazide - 43063-065-30 - (Lisinopril and Hydrochlorothiazide)

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Drug Information of Lisinopril with Hydrochlorothiazide

Product NDC: 43063-065
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: 43063-065
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076265
Marketing Category: ANDA
Start Marketing Date: 20020708

Package Information of Lisinopril with Hydrochlorothiazide

Package NDC: 43063-065-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (43063-065-30)

NDC Information of Lisinopril with Hydrochlorothiazide

NDC Code 43063-065-30
Proprietary Name Lisinopril with Hydrochlorothiazide
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (43063-065-30)
Product NDC 43063-065
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 PD-Rx Pharmaceuticals, 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 with Hydrochlorothiazide


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