Furosemide 42708-0123
Product NDC
42708-0123- Manufacturer
- Qpharma Inc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 1, 2006
- Listing Expires
- December 31, 2026
- Application
- ANDA077293
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Furosemide | 40 mg/1 |
Drug Class
Loop Diuretic [EPC]Increased Diuresis at Loop of Henle [PE]Loop Diuretic [EPC]
Packaging Options(1)
30 TABLET in 1 BOTTLE (42708-123-30)