Drugplain

bumetanide 1 mg/1

bumetanide · TABLET · Bryant Ranch Prepack

No Recall HistoryCurrently in Shortage
Plain English

bumetanide is a tablet containing bumetanide at 1 mg/1, taken oral. Manufactured by Bryant Ranch Prepack.

Key Facts

Brand Name
bumetanide
Generic Name
bumetanide
NDC Code (Product)
71335-1692
Manufacturer
Bryant Ranch Prepack
Strength
1 mg/1
Dosage Form
TABLET
Route
ORAL
Marketing Status
Application #
ANDA202900
Drug Class
Loop Diuretic [EPC]
Marketing Start
05/01/2018

Recall History

No Recall History

Side 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 1 mg/1?

The NDC (National Drug Code) for bumetanide 1 mg/1 is 71335-1692, listed by Bryant Ranch Prepack.

Product NDC

71335-1692

Package NDC

71335-1692-1

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)