NDC 64725-0265
Olanzapine 20 mg tablet, orally disintegrating
On the label: TYA Pharmaceuticals. It's repackaged: TYA Pharmaceuticals rebottles it from Dr.Reddy's Laboratories Ltd.'s NDC 55111-265.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Dr. Reddy's Laboratories Limited | Medchal-Malkajgiri, India | Makes it and tests it | Problems found, fixed voluntarilyOct 27, 2023 · 8 inspections |
Repackaging site
- TYA Pharmaceuticals, Location not on file · repackages it and relabels it
Product details
- Generic drug
- Olanzapine: every company that makes it
- Form
- tablet, orally disintegrating
- Strength
- 20 mg
- Approval
- ANDA ANDA076534
- On the market since
- Oct 24, 2011
- Package NDCs
64725-0265-1- Official label
- DailyMed (National Library of Medicine), updated Oct 30, 2013
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