NDC 42794-005 – Amiloride Hydrochloride

Amiloride Hydrochloride Anhydrous 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC42794-005

Product details

Brand name
Amiloride Hydrochloride
Generic name
Amiloride Hydrochloride
Labeler
Sigmapharm Laboratories, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA079133
Marketed since
June 14, 2021
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
42794-005-02100 TABLET in 1 BOTTLE (42794-005-02)Jun 14, 2021

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