NDC 42794-005

Amiloride Hydrochloride 5 mg tablet

On the label: SigmaPharm Laboratories, LLC.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Sigmapharm Laboratories, LLCBensalem, PA, United StatesMakes it and tests it Problems found, fixed voluntarilyDec 17, 2025 · 12 inspections

Product details

Generic drug
Amiloride: every company that makes it
Form
tablet, oral
Strength
5 mg
Approval
ANDA ANDA079133
On the market since
Jun 14, 2021
Package NDCs
42794-005-02
Official label
DailyMed (National Library of Medicine), updated Jan 10, 2023

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