NDC 81033-052
Torsemide 20 mg tablet
On the label: Kesin Pharma Corporation. It's repackaged: Kesin Pharma Corporation rebottles it from Camber Pharmaceuticals Inc.'s NDC 31722-531.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hetero Labs Limited | Hyderabad, India | Makes it, tests it and relabels it | Problems found, fixed voluntarilyJul 21, 2023 · 8 inspections |
Repackaging site
- Kesin Pharma Corporation, Oldsmar, FL, United States · labels it and repackages it
Product details
- Generic drug
- Torsemide: every company that makes it
- Form
- tablet, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA079234
- On the market since
- Jan 1, 2011
- Package NDCs
81033-052-51- Official label
- DailyMed (National Library of Medicine), updated Nov 9, 2026
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