NDC 0574-0292 – Amiloride hydrochloride

Amiloride Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC0574-0292

Product details

Brand name
Amiloride hydrochloride
Generic name
Amiloride hydrochloride
Labeler
Padagis US LLC
Dosage form
Tablet
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA018200
Marketed since
April 6, 2009
Listing expires
December 31, 2026
Pharmacologic class
Potassium-sparing Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Amiloride hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
0574-0292-01100 TABLET in 1 BOTTLE (0574-0292-01)Apr 6, 2009

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