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Amiloride Hydrochloride and Hydrochlorothiazide - 0555-0483-05 - (Amiloride Hydrochloride and Hydrochlorothiazide)

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Drug Information of Amiloride Hydrochloride and Hydrochlorothiazide

Product NDC: 0555-0483
Proprietary Name: Amiloride Hydrochloride and Hydrochlorothiazide
Non Proprietary Name: Amiloride Hydrochloride and Hydrochlorothiazide
Active Ingredient(s): 5; 50    mg/1; mg/1 & nbsp;   Amiloride Hydrochloride and Hydrochlorothiazide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Amiloride Hydrochloride and Hydrochlorothiazide

Product NDC: 0555-0483
Labeler Name: Barr Laboratories Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071111
Marketing Category: ANDA
Start Marketing Date: 19891201

Package Information of Amiloride Hydrochloride and Hydrochlorothiazide

Package NDC: 0555-0483-05
Package Description: 1000 TABLET in 1 BOTTLE (0555-0483-05)

NDC Information of Amiloride Hydrochloride and Hydrochlorothiazide

NDC Code 0555-0483-05
Proprietary Name Amiloride Hydrochloride and Hydrochlorothiazide
Package Description 1000 TABLET in 1 BOTTLE (0555-0483-05)
Product NDC 0555-0483
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amiloride Hydrochloride and Hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19891201
Marketing Category Name ANDA
Labeler Name Barr Laboratories Inc.
Substance Name AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Strength Number 5; 50
Strength Unit mg/1; mg/1
Pharmaceutical Classes Decreased Renal K+ Excretion [PE],Increased Diuresis [PE],Potassium-sparing Diuretic [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]

Complete Information of Amiloride Hydrochloride and Hydrochlorothiazide


General Information