Amiloride Hydrochloride And Hydrochlorothiazide 00555-0483
Product NDC
00555-0483- Manufacturer
- Teva Pharmaceuticals Usa, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 1, 1989
- Listing Expires
- December 31, 2026
- Application
- ANDA071111
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Amiloride Hydrochloride | 5 mg/1 |
| Hydrochlorothiazide | 50 mg/1 |
Drug Class
Thiazide Diuretic [EPC]Decreased Renal K+ Excretion [PE]Increased Diuresis [PE]
Packaging Options(2)
100 TABLET in 1 BOTTLE (0555-0483-02)
1000 TABLET in 1 BOTTLE (0555-0483-05)