NDC 53808-0302
Sulindac 200 mg tablet
On the label: State of Florida DOH Central Pharmacy. It's repackaged: State of Florida DOH Central Pharmacy rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 53489-479.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Frontida BioPharm, LLC | Philadelphia, PA, United States | Makes it, tests it and packages it | No problems foundApr 2, 2026 · 10 inspections, 1 with FDA action |
Product details
- Generic drug
- Sulindac: every company that makes it
- Form
- tablet
- Strength
- 200 mg
- Approval
- ANDA ANDA072051
- On the market since
- Jul 1, 2009
- Package NDCs
53808-0302-1- Official label
- DailyMed (National Library of Medicine), updated May 21, 2010
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