Hydrochlorothiazide 72162-1357
Product NDC
72162-1357- Manufacturer
- Bryant Ranch Prepack
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 29, 2002
- Listing Expires
- December 31, 2026
- Application
- ANDA040412
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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(1)
100 TABLET in 1 BOTTLE, PLASTIC (72162-1357-1)