Furosemide 51655-0269
Product NDC
51655-0269- Manufacturer
- Northwind Health Company, Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 8, 2022
- Listing Expires
- December 31, 2027
- Application
- ANDA077293
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Furosemide | 20 mg/1 |
Drug Class
Loop Diuretic [EPC]Increased Diuresis at Loop of Henle [PE]Loop Diuretic [EPC]
Packaging Options(4)
60 TABLET in 1 BOTTLE, PLASTIC (51655-269-25)
90 TABLET in 1 BOTTLE, PLASTIC (51655-269-26)
30 TABLET in 1 BOTTLE, PLASTIC (51655-269-52)
10 TABLET in 1 BOTTLE, PLASTIC (51655-269-53)