NDC 42806-011

Sulindac 200 mg tablet

On the label: Epic Pharma, LLC.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Epic Pharma, LLCLaurelton, NY, United StatesMakes it Problems found, fixed voluntarilyJun 12, 2026 · 14 inspections

Recalls

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, oral
Strength
200 mg
Approval
ANDA ANDA072711
On the market since
Jan 25, 2010
Package NDCs
42806-011-01 42806-011-05 42806-011-10
Official label
DailyMed (National Library of Medicine), updated Dec 20, 2024

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