NDC 50090-0529

Sulindac 200 mg tablet

On the label: A-S Medication Solutions. It's repackaged: A-S Medication Solutions rebottles it from Epic Pharma, LLC's NDC 42806-011.

United States: 1

Where the pills inside were made

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

Repackaging site

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
50090-0529-0 50090-0529-1 50090-0529-4
Official label
DailyMed (National Library of Medicine), updated May 8, 2026

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