Hydrochlorothiazide 71205-0751
Product NDC
71205-0751- Manufacturer
- Proficient Rx Lp
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 7, 1980
- Listing Expires
- December 31, 2026
- Application
- ANDA083177
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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(3)
30 TABLET in 1 BOTTLE (71205-751-30)
60 TABLET in 1 BOTTLE (71205-751-60)
90 TABLET in 1 BOTTLE (71205-751-90)