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Amiloride Hydrochloride and Hydrochlorothiazide - 54868-0667-2 - (Amiloride Hydrochloride and Hydrochlorothiazide)

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Drug Information of Amiloride Hydrochloride and Hydrochlorothiazide

Product NDC: 54868-0667
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: 54868-0667
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073209
Marketing Category: ANDA
Start Marketing Date: 19960516

Package Information of Amiloride Hydrochloride and Hydrochlorothiazide

Package NDC: 54868-0667-2
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC (54868-0667-2)

NDC Information of Amiloride Hydrochloride and Hydrochlorothiazide

NDC Code 54868-0667-2
Proprietary Name Amiloride Hydrochloride and Hydrochlorothiazide
Package Description 90 TABLET in 1 BOTTLE, PLASTIC (54868-0667-2)
Product NDC 54868-0667
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amiloride Hydrochloride and Hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19960516
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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


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