NDC 53808-0814
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 Epic Pharma, LLC's NDC 42806-011.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Epic Pharma, LLC | Laurelton, NY, United States | Makes it | Problems found, fixed voluntarilyJun 12, 2026 · 14 inspections |
Repackaging site
- State of Florida DOH Central Pharmacy, Location not on file · repackages it
Recalls
- Mar 15, 2021 · Class II · Cardinal Health Inc.
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Lots: 1578F201
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Sulindac: every company that makes it
- Form
- tablet
- Strength
- 200 mg
- Approval
- ANDA ANDA072711
- On the market since
- Jan 1, 2013
- Package NDCs
53808-0814-1- Official label
- DailyMed (National Library of Medicine), updated Sep 30, 2013
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?