NDC 0555-0483 – Amiloride Hydrochloride and Hydrochlorothiazide
Amiloride Hydrochloride 5 mg/1; Hydrochlorothiazide 50 mg/1 · Tablet · Oral
Product NDC0555-0483
Product details
- Brand name
- Amiloride Hydrochloride and Hydrochlorothiazide
- Generic name
- Amiloride Hydrochloride and Hydrochlorothiazide
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA071111
- Marketed since
- December 1, 1989
- Listing expires
- December 31, 2026
- Pharmacologic class
- Potassium-sparing Diuretic; Thiazide Diuretic
Active ingredients
- Amiloride Hydrochloride 5 mg/1
- Hydrochlorothiazide 50 mg/1
Uses, dosage, side effects and warnings for Amiloride Hydrochloride and Hydrochlorothiazide →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 0555-0483-02 | 100 TABLET in 1 BOTTLE (0555-0483-02) | Dec 1, 1989 |
| 0555-0483-05 | 1000 TABLET in 1 BOTTLE (0555-0483-05) | Dec 1, 1989 |