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Lisinopril and Hydrochlorothiazide - 49349-209-02 - (Lisinopril and Hydrochlorothiazide)

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Drug Information of Lisinopril and Hydrochlorothiazide

Product NDC: 49349-209
Proprietary Name: Lisinopril and 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 and Hydrochlorothiazide

Product NDC: 49349-209
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076194
Marketing Category: ANDA
Start Marketing Date: 20110422

Package Information of Lisinopril and Hydrochlorothiazide

Package NDC: 49349-209-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-209-02)

NDC Information of Lisinopril and Hydrochlorothiazide

NDC Code 49349-209-02
Proprietary Name Lisinopril and Hydrochlorothiazide
Package Description 30 TABLET in 1 BLISTER PACK (49349-209-02)
Product NDC 49349-209
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lisinopril and Hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110422
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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 and Hydrochlorothiazide


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