NDC 67296-2262

Olanzapine 5 mg tablet, film coated

On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. rebottles it from Northstar Rx LLC.'s NDC 72603-155.

India: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Macleods Pharmaceuticals LimitedDistrict Solan, IndiaMakes it, tests it, packages it and labels it Problems found, fixed voluntarilyOct 20, 2023 · 6 inspections, 2 with FDA action

Repackaging site

Product details

Generic drug
Olanzapine: every company that makes it
Form
tablet, film coated, oral
Strength
5 mg
Approval
ANDA ANDA202862
On the market since
Aug 22, 2014
Package NDCs
67296-2262-3
Official label
DailyMed (National Library of Medicine), updated Jun 20, 2026

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