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Lisinopril and hydrochlorothiazide - 21695-735-30 - (Lisinopril and hydrochlorothiazide)

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Drug Information of Lisinopril and hydrochlorothiazide

Product NDC: 21695-735
Proprietary Name: Lisinopril and hydrochlorothiazide
Non Proprietary Name: Lisinopril and hydrochlorothiazide
Active Ingredient(s): 25; 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: 21695-735
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076194
Marketing Category: ANDA
Start Marketing Date: 20030301

Package Information of Lisinopril and hydrochlorothiazide

Package NDC: 21695-735-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (21695-735-30)

NDC Information of Lisinopril and hydrochlorothiazide

NDC Code 21695-735-30
Proprietary Name Lisinopril and hydrochlorothiazide
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (21695-735-30)
Product NDC 21695-735
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lisinopril and hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20030301
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name HYDROCHLOROTHIAZIDE; LISINOPRIL
Strength Number 25; 20
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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