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Fosinopril Sodium and Hydrochlorothiazide - 0185-0341-01 - (Fosinopril Sodium and Hydrochlorothiazide)

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Drug Information of Fosinopril Sodium and Hydrochlorothiazide

Product NDC: 0185-0341
Proprietary Name: Fosinopril Sodium and Hydrochlorothiazide
Non Proprietary Name: Fosinopril Sodium and Hydrochlorothiazide
Active Ingredient(s): 10; 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: 0185-0341
Labeler Name: Eon Labs, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076961
Marketing Category: ANDA
Start Marketing Date: 20050928

Package Information of Fosinopril Sodium and Hydrochlorothiazide

Package NDC: 0185-0341-01
Package Description: 100 TABLET in 1 BOTTLE (0185-0341-01)

NDC Information of Fosinopril Sodium and Hydrochlorothiazide

NDC Code 0185-0341-01
Proprietary Name Fosinopril Sodium and Hydrochlorothiazide
Package Description 100 TABLET in 1 BOTTLE (0185-0341-01)
Product NDC 0185-0341
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fosinopril Sodium and Hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20050928
Marketing Category Name ANDA
Labeler Name Eon Labs, 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


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