Bumetanide 81469-0222
Product NDC
81469-0222- Manufacturer
- First Nation Group, Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 19, 2026
- Listing Expires
- December 31, 2027
- Application
- ANDA219291
Need to source Bumetanide? Find it on a pharmacy-to-pharmacy marketplace at better prices.
✓ DSCSA Compliant. ✓ Verified Pharmacies Only.P2P pharmacy marketplace.
Active Ingredients
| Ingredient | Strength |
|---|---|
| Bumetanide | 1 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 (81469-222-01)
500 TABLET in 1 BOTTLE (81469-222-05)