NDC 82804-287
Bumetanide 1 mg tablet
On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP rebottles it from Solco Healthcare U.S., LLC's NDC 43547-897.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Appco Pharma LLC | Piscataway, NJ, United States | Makes it | Problems found, fixed voluntarilyMay 14, 2026 · 9 inspections |
Repackaging site
- Proficient Rx LP, Thousand Oaks, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Bumetanide: every company that makes it
- Form
- tablet, oral
- Strength
- 1 mg
- Approval
- ANDA ANDA212931
- On the market since
- Mar 1, 2025
- Package NDCs
82804-287-30- Official label
- DailyMed (National Library of Medicine), updated Apr 1, 2026
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