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Benazepril Hydrochloride and Hydrochlorothiazide - 63629-1809-1 - (Benazepril Hydrochloride and Hydrochlorothiazide)

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Drug Information of Benazepril Hydrochloride and Hydrochlorothiazide

Product NDC: 63629-1809
Proprietary Name: Benazepril Hydrochloride and Hydrochlorothiazide
Non Proprietary Name: Benazepril Hydrochloride and Hydrochlorothiazide
Active Ingredient(s): 10; 12.5    mg/1; mg/1 & nbsp;   Benazepril Hydrochloride and Hydrochlorothiazide
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Benazepril Hydrochloride and Hydrochlorothiazide

Product NDC: 63629-1809
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076631
Marketing Category: ANDA
Start Marketing Date: 20040211

Package Information of Benazepril Hydrochloride and Hydrochlorothiazide

Package NDC: 63629-1809-1
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (63629-1809-1)

NDC Information of Benazepril Hydrochloride and Hydrochlorothiazide

NDC Code 63629-1809-1
Proprietary Name Benazepril Hydrochloride and Hydrochlorothiazide
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (63629-1809-1)
Product NDC 63629-1809
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Benazepril Hydrochloride and Hydrochlorothiazide
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20040211
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Strength Number 10; 12.5
Strength Unit mg/1; mg/1
Pharmaceutical Classes Angiontensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]

Complete Information of Benazepril Hydrochloride and Hydrochlorothiazide


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