Spironolactone And Hydrochlorothiazide 53489-0144
Product NDC
53489-0144- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 2, 1987
- Listing Expires
- December 31, 2026
- Application
- ANDA089534
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydrochlorothiazide | 25 mg/1 |
| Spironolactone | 25 mg/1 |
Drug Class
Thiazide Diuretic [EPC]Aldosterone Antagonist [EPC]Aldosterone Antagonist [EPC]
Packaging Options(3)
100 TABLET in 1 BOTTLE, PLASTIC (53489-144-01)
500 TABLET in 1 BOTTLE, PLASTIC (53489-144-05)
1000 TABLET in 1 BOTTLE, PLASTIC (53489-144-10)