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Fosinopril Sodium and Hydrochlorothiazide - 65862-309-99 - (Fosinopril Sodium and Hydrochlorothiazide)

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Drug Information of Fosinopril Sodium and Hydrochlorothiazide

Product NDC: 65862-309
Proprietary Name: Fosinopril Sodium and Hydrochlorothiazide
Non Proprietary Name: Fosinopril Sodium and Hydrochlorothiazide
Active Ingredient(s): 20; 12.5    mg/1; mg/1 & nbsp;   Fosinopril Sodium and Hydrochlorothiazide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Fosinopril Sodium and Hydrochlorothiazide

Product NDC: 65862-309
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079245
Marketing Category: ANDA
Start Marketing Date: 20090709

Package Information of Fosinopril Sodium and Hydrochlorothiazide

Package NDC: 65862-309-99
Package Description: 1000 TABLET in 1 BOTTLE (65862-309-99)

NDC Information of Fosinopril Sodium and Hydrochlorothiazide

NDC Code 65862-309-99
Proprietary Name Fosinopril Sodium and Hydrochlorothiazide
Package Description 1000 TABLET in 1 BOTTLE (65862-309-99)
Product NDC 65862-309
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fosinopril Sodium and Hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090709
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
Substance Name FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE
Strength Number 20; 12.5
Strength Unit mg/1; mg/1
Pharmaceutical Classes Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]

Complete Information of Fosinopril Sodium and Hydrochlorothiazide


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