NDC 54868-6364
Olanzapine 7.5 mg tablet, film coated
On the label: Physicians Total Care, Inc.. It's repackaged from NDC 0093-5769, made by Teva Pharmaceuticals USA, Inc. (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 Physicians Total Care, Inc. names for other drugs.
Product details
- Generic drug
- Olanzapine: every company that makes it
- Form
- tablet, film coated
- Strength
- 7.5 mg
- Approval
- ANDA ANDA076000
- On the market since
- Aug 22, 2012
- Package NDCs
54868-6364-0- Official label
- DailyMed (National Library of Medicine), updated Aug 10, 2012
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