Hydrochlorothiazide 42708-0164
Product NDC
42708-0164- Manufacturer
- Qpharma Inc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 15, 2015
- Listing Expires
- December 31, 2026
- Application
- ANDA085182
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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(1)
30 TABLET in 1 BOTTLE, PLASTIC (42708-164-30)