NDC 71335-2674 – Spironolactone and Hydrochlorothiazide
Spironolactone 25 mg/1; Hydrochlorothiazide 25 mg/1 · Tablet · Oral
Product NDC71335-2674
Product details
- Brand name
- Spironolactone and Hydrochlorothiazide
- Generic name
- Spironolactone and Hydrochlorothiazide
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA089534
- Marketed since
- July 2, 1987
- Listing expires
- December 31, 2026
- Pharmacologic class
- Aldosterone Antagonist; Thiazide Diuretic
Active ingredients
- Spironolactone 25 mg/1
- Hydrochlorothiazide 25 mg/1
Uses, dosage, side effects and warnings for Spironolactone and Hydrochlorothiazide →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 71335-2674-1 | 100 TABLET in 1 BOTTLE (71335-2674-1) | Jun 26, 2025 |
| 71335-2674-2 | 30 TABLET in 1 BOTTLE (71335-2674-2) | Jun 26, 2025 |
| 71335-2674-3 | 60 TABLET in 1 BOTTLE (71335-2674-3) | Jun 26, 2025 |
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