bumetanide 2 mg/1
bumetanide · TABLET · Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
No Recall HistoryCurrently in Shortage
Plain English
bumetanide is a tablet containing bumetanide at 2 mg/1, taken oral. Manufactured by Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc..
Key Facts
- Brand Name
- bumetanide
- Generic Name
- bumetanide
- NDC Code (Product)
23155-902- Manufacturer
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- Strength
- 2 mg/1
- Dosage Form
- TABLET
- Route
- ORAL
- Marketing Status
- Application #
- ANDA074225
- Drug Class
- Loop Diuretic [EPC]
- Marketing Start
- 06/28/2024
Recall History
No Recall HistorySide Effects Reported to FDA
FDA FAERS database · These are reported events, not confirmed side effects
dyspnoea1,845 reports
acute kidney injury1,373 reports
fatigue1,251 reports
death1,237 reports
diarrhoea1,155 reports
nausea1,068 reports
dizziness921 reports
headache879 reports
pneumonia812 reports
renal failure737 reports
Frequently Asked Questions
What is bumetanide used for?
bumetanide contains bumetanide. It is a tablet taken oral. Consult your doctor for specific uses.
Is bumetanide a controlled substance?
bumetanide is not classified as a controlled substance by the DEA.
What is the generic name for bumetanide?
The generic name for bumetanide is bumetanide. There are 7 other brand versions of bumetanide.
What is the NDC code for bumetanide 2 mg/1?
The NDC (National Drug Code) for bumetanide 2 mg/1 is 23155-902, listed by Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc..