NDC 64725-0552
Olanzapine 5 mg tablet
On the label: TYA Pharmaceuticals. It's repackaged from NDC 62756-552, made by Sun Pharmaceutical Industries Limited (Olanzapine). That product's FDA listing has since ended, so its label and factories are no longer published.
Where the pills inside were made
This label doesn't name the factory that makes the drug (it lists 1 site that relabels it). Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants TYA Pharmaceuticals names for other drugs.
Product details
- Generic drug
- Olanzapine: every company that makes it
- Form
- tablet
- Strength
- 5 mg
- Approval
- ANDA ANDA091038
- On the market since
- Apr 23, 2012
- Package NDCs
64725-0552-1- Official label
- DailyMed (National Library of Medicine), updated Apr 26, 2012
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?