Hydrochlorothiazide 68071-4933
Product NDC
68071-4933- Manufacturer
- Nucare Pharmaceuticals,inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 2, 2009
- Listing Expires
- December 31, 2026
- Application
- ANDA040907
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydrochlorothiazide | 25 mg/1 |
Drug Class
Thiazide Diuretic [EPC]Increased Diuresis [PE]Thiazide Diuretic [EPC]
Packaging Options(2)
20 TABLET in 1 BOTTLE (68071-4933-7)
90 TABLET in 1 BOTTLE (68071-4933-9)