Hydrochlorothiazide 70518-4359
Product NDC
70518-4359- Manufacturer
- Remedyrepack Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 16, 2025
- 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(3)
15 TABLET in 1 BOTTLE, PLASTIC (70518-4359-0)
30 TABLET in 1 BLISTER PACK (70518-4359-1)
90 TABLET in 1 BOTTLE, PLASTIC (70518-4359-2)