Hydrochlorothiazide 68788-8813
Product NDC
68788-8813- Manufacturer
- Preferred Pharmaceuticals Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 21, 2025
- Listing Expires
- December 31, 2026
- Application
- ANDA040702
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydrochlorothiazide | 12.5 mg/1 |
Drug Class
Thiazide Diuretic [EPC]Increased Diuresis [PE]Thiazide Diuretic [EPC]
Packaging Options(5)
7 TABLET in 1 BOTTLE, PLASTIC (68788-8813-1)
30 TABLET in 1 BOTTLE, PLASTIC (68788-8813-3)
60 TABLET in 1 BOTTLE, PLASTIC (68788-8813-6)
100 TABLET in 1 BOTTLE, PLASTIC (68788-8813-8)
90 TABLET in 1 BOTTLE, PLASTIC (68788-8813-9)