amiloride hydrochloride
Active substance: amiloride
TABLET · AMILORIDE HYDROCHLORIDE 5 mg/1
United StatesActive
Marketing holder: Padagis US LLC
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
- Countries with the substance registered: 1
Composition
- AMILORIDE HYDROCHLORIDE · 5 mg/1
Import and control
Control by country
- United Statesprescription only
Source: openFDA NDC · record 01a1208c-6594-7a8b-8277-3cae6671924a,01a12093-69cb-741a-b737-d93887a2b6b8,01a1209c-271c-7403-abf5-60cacfc45dd5;count=3 · valid from 2026-10-09 · verified 2026-10-09
Registration
- Registration number
- 0574-0292
- Registration status
- Active
- Dispensing
- Prescription only
- Route
- ORAL
Sources
- product · openFDA NDC · 0574-0292 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 0574-0292 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 0574-0292 · Verified 2026-10-09 · open in source