Amiloride Hydrochloride And Hydrochlorothiazide 00555-0483-02

Package NDC

00555-0483-02

Manufacturer: Teva Pharmaceuticals Usa, Inc.
Dosage Form: Tablet
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: December 1, 1989
Listing Expires: December 31, 2026
Application: ANDA071111

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Active Ingredients

Ingredient	Strength
Amiloride Hydrochloride	5 mg/1
Hydrochlorothiazide	50 mg/1

Drug Class

Thiazide Diuretic [EPC]Decreased Renal K+ Excretion [PE]Increased Diuresis [PE]

Selected Package

00555-0483-02Selected

100 TABLET in 1 BOTTLE (0555-0483-02)

Other packages for this product(1)

00555-0483-05

1000 TABLET in 1 BOTTLE (0555-0483-05)

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