Hydrochlorothiazide 68788-7790
Product NDC
68788-7790- Manufacturer
- Preferred Pharmaceuticals Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 21, 2020
- Listing Expires
- December 31, 2027
- Application
- ANDA085182
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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(5)
100 TABLET in 1 BOTTLE (68788-7790-0)
15 TABLET in 1 BOTTLE (68788-7790-1)
30 TABLET in 1 BOTTLE (68788-7790-3)
60 TABLET in 1 BOTTLE (68788-7790-6)
90 TABLET in 1 BOTTLE (68788-7790-9)