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LISINOPRIL AND HYDROCHLOROTHIAZIDE - 68788-9807-9 - (LISINOPRIL AND HYDROCHLOROTHIAZIDE)

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Drug Information of LISINOPRIL AND HYDROCHLOROTHIAZIDE

Product NDC: 68788-9807
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: 68788-9807
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077912
Marketing Category: ANDA
Start Marketing Date: 20120423

Package Information of LISINOPRIL AND HYDROCHLOROTHIAZIDE

Package NDC: 68788-9807-9
Package Description: 90 TABLET in 1 BOTTLE (68788-9807-9)

NDC Information of LISINOPRIL AND HYDROCHLOROTHIAZIDE

NDC Code 68788-9807-9
Proprietary Name LISINOPRIL AND HYDROCHLOROTHIAZIDE
Package Description 90 TABLET in 1 BOTTLE (68788-9807-9)
Product NDC 68788-9807
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name LISINOPRIL AND HYDROCHLOROTHIAZIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120423
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, 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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