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Last Updated: December 12, 2025

Details for New Drug Application (NDA): 073334

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NDA 073334 describes AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE, which is a drug marketed by Barr, Chartwell Rx, Rising, Teva, and Watson Labs, and is included in five NDAs. It is available from one supplier. Additional details are available on the AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE profile page.

The generic ingredient in AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE is amiloride hydrochloride; hydrochlorothiazide. There are five drug master file entries for this compound. One supplier is listed for this compound. Additional details are available on the amiloride hydrochloride; hydrochlorothiazide profile page.

Summary for 073334

Tradename:	AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
Applicant:	Watson Labs
Ingredient:	amiloride hydrochloride; hydrochlorothiazide
Patents:	0

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	TABLET;ORAL			Strength	EQ 5MG ANHYDROUS;50MG
Approval Date:	Jul 19, 1991	TE:		RLD:	No

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