Hydrochlorothiazide 69584-0361
Product NDC
69584-0361- Manufacturer
- Oxford Pharmaceuticals, Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 25, 2020
- Listing Expires
- December 31, 2026
- Application
- ANDA087059
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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(3)
100 TABLET in 1 BOTTLE (69584-361-10)
1000 TABLET in 1 BOTTLE (69584-361-90)
5000 TABLET in 1 BOTTLE (69584-361-95)