NDC 67046-0363
Olanzapine 7.5 mg tablet, film coated
On the label: Coupler LLC. It's repackaged: Coupler LLC rebottles it from Dr. Reddy's Laboratories Inc.'s NDC 43598-165.
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
- Coupler LLC, West Chester, PA, United States · repackages it
Product details
- Generic drug
- Olanzapine: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 7.5 mg
- Approval
- ANDA ANDA076255
- On the market since
- Jun 10, 2026
- Package NDCs
67046-0363-3- Official label
- DailyMed (National Library of Medicine), updated Jun 10, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?