Hydrochlorothiazide 51655-0272
Product NDC
51655-0272- Manufacturer
- Northwind Health Company, Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 4, 2020
- Listing Expires
- December 31, 2027
- 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(2)
90 TABLET in 1 BOTTLE, PLASTIC (51655-272-26)
30 TABLET in 1 BOTTLE, PLASTIC (51655-272-52)