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Fosinopril Sodium and Hydrochlorothiazide - 23155-060-01 - (Fosinopril Sodium and Hydrochlorothiazide Tablet)

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Drug Information of Fosinopril Sodium and Hydrochlorothiazide

Product NDC: 23155-060
Proprietary Name: Fosinopril Sodium and Hydrochlorothiazide
Non Proprietary Name: Fosinopril Sodium and Hydrochlorothiazide Tablet
Active Ingredient(s): 10; 12.5    mg/1; mg/1 & nbsp;   Fosinopril Sodium and Hydrochlorothiazide Tablet
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Fosinopril Sodium and Hydrochlorothiazide

Product NDC: 23155-060
Labeler Name: Heritage Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079025
Marketing Category: ANDA
Start Marketing Date: 20111115

Package Information of Fosinopril Sodium and Hydrochlorothiazide

Package NDC: 23155-060-01
Package Description: 100 TABLET in 1 BOTTLE (23155-060-01)

NDC Information of Fosinopril Sodium and Hydrochlorothiazide

NDC Code 23155-060-01
Proprietary Name Fosinopril Sodium and Hydrochlorothiazide
Package Description 100 TABLET in 1 BOTTLE (23155-060-01)
Product NDC 23155-060
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fosinopril Sodium and Hydrochlorothiazide Tablet
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111115
Marketing Category Name ANDA
Labeler Name Heritage Pharmaceuticals Inc.
Substance Name FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE
Strength Number 10; 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


General Information