NDC 76282-799

Bumetanide 2 mg tablet

On the label: Exelan Pharmaceuticals, Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Appco Pharma LLCPiscataway, NJ, United StatesMakes it and packages it Problems found, fixed voluntarilyMay 14, 2026 · 9 inspections

Product details

Generic drug
Bumetanide: every company that makes it
Form
tablet, oral
Strength
2 mg
Approval
ANDA ANDA212931
On the market since
Mar 1, 2025
Package NDCs
76282-799-01 76282-799-05
Official label
DailyMed (National Library of Medicine), updated Jan 27, 2026

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