NDC 64725-0955

Olanzapine 10 mg per 2 mL injection, powder, lyophilized, for solution

On the label: TYA Pharmaceuticals. It's repackaged: TYA Pharmaceuticals rebottles it from American Regent, Inc.'s NDC 0517-0955.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
American Regent, Inc.New Albany, OH, United StatesMakes it Problems found, fixed voluntarilyJan 29, 2026 · 5 inspections

Repackaging site

Product details

Generic drug
Olanzapine: every company that makes it
Form
injection, powder, lyophilized, for solution
Strength
10 mg per 2 mL
Approval
ANDA ANDA201741
On the market since
Jun 27, 2012
Package NDCs
64725-0955-1
Official label
DailyMed (National Library of Medicine), updated Jul 5, 2012

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