Furosemide 70518-4679
Product NDC
70518-4679- Manufacturer
- Remedyrepack Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 22, 2026
- Listing Expires
- December 31, 2027
- Application
- ANDA078010
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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(1)
30 TABLET in 1 BLISTER PACK (70518-4679-0)