NDC 42582-113

Ibuprofen 800 mg tablet

On the label: Bi-Coastal Pharma International LLC.

Where it's made

This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Bi-Coastal Pharma International LLC names for other drugs.

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
Ibuprofen: every company that makes it
Form
tablet
Strength
800 mg
Approval
ANDA ANDA090796
On the market since
Apr 14, 2016
Package NDCs
42582-113-10 42582-113-18
Official label
DailyMed (National Library of Medicine), updated Apr 14, 2016

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