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Fosinopril Sodium and Hydrochlorothiazide - 63304-403-10 - (Fosinopril Sodium and Hydrocholorothiazide)

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Drug Information of Fosinopril Sodium and Hydrochlorothiazide

Product NDC: 63304-403
Proprietary Name: Fosinopril Sodium and Hydrochlorothiazide
Non Proprietary Name: Fosinopril Sodium and Hydrocholorothiazide
Active Ingredient(s): 10; 12.5    mg/1; mg/1 & nbsp;   Fosinopril Sodium and Hydrocholorothiazide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Fosinopril Sodium and Hydrochlorothiazide

Product NDC: 63304-403
Labeler Name: Ranbaxy Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076739
Marketing Category: ANDA
Start Marketing Date: 20041220

Package Information of Fosinopril Sodium and Hydrochlorothiazide

Package NDC: 63304-403-10
Package Description: 1000 TABLET in 1 BOTTLE (63304-403-10)

NDC Information of Fosinopril Sodium and Hydrochlorothiazide

NDC Code 63304-403-10
Proprietary Name Fosinopril Sodium and Hydrochlorothiazide
Package Description 1000 TABLET in 1 BOTTLE (63304-403-10)
Product NDC 63304-403
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fosinopril Sodium and Hydrocholorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20041220
Marketing Category Name ANDA
Labeler Name Ranbaxy 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