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Fosinopril Sodium and Hydrochlorothiazide - 23155-061-05 - (Fosinopril Sodium and Hydrochlorothiazide)

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Drug Information of Fosinopril Sodium and Hydrochlorothiazide

Product NDC: 23155-061
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: 23155-061
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: 23155-061-05
Package Description: 500 TABLET in 1 BOTTLE (23155-061-05)

NDC Information of Fosinopril Sodium and Hydrochlorothiazide

NDC Code 23155-061-05
Proprietary Name Fosinopril Sodium and Hydrochlorothiazide
Package Description 500 TABLET in 1 BOTTLE (23155-061-05)
Product NDC 23155-061
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fosinopril Sodium and Hydrochlorothiazide
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 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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