Bumetanide 00781-8099
Product NDC
00781-8099- Manufacturer
- Sandoz Inc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 3, 2026
- Listing Expires
- December 31, 2027
- Application
- ANDA074700
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Bumetanide | .5 mg/1 |
Drug Class
Loop Diuretic [EPC]Increased Diuresis at Loop of Henle [PE]Loop Diuretic [EPC]
Packaging Options(2)
100 TABLET in 1 BOTTLE (0781-8099-01)
500 TABLET in 1 BOTTLE (0781-8099-05)