Amiloride Hydrochloride 49884-0117-10

Package NDC

49884-0117-10

Manufacturer: Endo Usa, Inc.
Dosage Form: Tablet
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: January 22, 1986
Listing Expires: December 31, 2026
Application: ANDA070346

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Active Ingredients

Ingredient	Strength
Amiloride Hydrochloride Anhydrous	5 mg/1

Drug Class

Decreased Renal K+ Excretion [PE]Increased Diuresis [PE]Potassium-sparing Diuretic [EPC]

Selected Package

49884-0117-10Selected

1000 TABLET in 1 BOTTLE (49884-117-10)

Other packages for this product(1)

49884-0117-01

100 TABLET in 1 BOTTLE (49884-117-01)

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