NDC 71335-2202 – Spironolactone and Hydrochlorothiazide
Spironolactone 25 mg/1; Hydrochlorothiazide 25 mg/1 · Tablet · Oral
Product NDC71335-2202
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, 2027
- 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 (1)
| Package NDC | Description | Since |
|---|---|---|
| 71335-2202-1 | 100 TABLET in 1 BOTTLE, PLASTIC (71335-2202-1) | Aug 4, 2023 |
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