NDC 70518-1635
Olanzapine 10 mg tablet, film coated
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Dr. Reddy's Laboratories Inc.'s NDC 43598-166.
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 |
Product details
- Generic drug
- Olanzapine: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 10 mg
- Approval
- ANDA ANDA076255
- On the market since
- Nov 6, 2018
- Package NDCs
70518-1635-070518-1635-170518-1635-2- Official label
- DailyMed (National Library of Medicine), updated Sep 21, 2026
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