Hydrochlorothiazide 65862-0134
Product NDC
65862-0134- Manufacturer
- Aurobindo Pharma Limited
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 20, 2007
- Listing Expires
- December 31, 2026
- Application
- ANDA040780
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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)
100 TABLET in 1 BOTTLE (65862-134-01)
1000 TABLET in 1 BOTTLE (65862-134-99)