NDC 65162-360

Mesalamine 800 mg tablet, delayed release

On the label: Amneal Pharmaceuticals.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Amneal Pharmaceuticals of New York, LLCBrookhaven, NY, United StatesMakes it, tests it, packages it and labels it No problems foundSep 25, 2026 · 14 inspections

Product details

Generic drug
Mesalamine: every company that makes it
Form
tablet, delayed release, oral
Strength
800 mg
Approval
ANDA ANDA215067
On the market since
Feb 19, 2025
Package NDCs
65162-360-18
Official label
DailyMed (National Library of Medicine), updated Sep 16, 2026

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