NDC 48792-7811

Ibuprofen 800 mg tablet, film coated

On the label: Sunshine Lake Pharma Co., Ltd..

China: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Sunshine Lake Pharma Co., Ltd.Dongguan, ChinaMakes it Problems found, fixed voluntarilyMar 22, 2024 · 5 inspections, 1 with FDA action

Product details

Generic drug
Ibuprofen: every company that makes it
Form
tablet, film coated
Strength
800 mg
Approval
ANDA ANDA204062
On the market since
Sep 10, 2018
Package NDCs
48792-7811-1
Official label
DailyMed (National Library of Medicine), updated Dec 8, 2024

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