Hydrochlorothiazide 50228-0112
Product NDC
50228-0112- Manufacturer
- Sciegen Pharmaceuticals, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 5, 2014
- Listing Expires
- December 31, 2026
- Application
- ANDA203018
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydrochlorothiazide | 50 mg/1 |
Drug Class
Thiazide Diuretic [EPC]Increased Diuresis [PE]Thiazide Diuretic [EPC]
Packaging Options(2)
1000 TABLET in 1 BOTTLE (50228-112-10)
30 TABLET in 1 BOTTLE (50228-112-30)