Amiloride Hydrochloride 63629-2114
Product NDC
63629-2114- Manufacturer
- Bryant Ranch Prepack
- 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]
Packaging Options(1)
1000 TABLET in 1 BOTTLE (63629-2114-1)