NDC 50090-3958
Olanzapine 10 mg tablet, orally disintegrating
On the label: A-S Medication Solutions. It's repackaged from NDC 49884-321, made by Endo 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 repackages it and 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 A-S Medication Solutions names for other drugs.
Product details
- Generic drug
- Olanzapine: every company that makes it
- Form
- tablet, orally disintegrating
- Strength
- 10 mg
- Approval
- ANDA ANDA078109
- On the market since
- Oct 24, 2011
- Package NDCs
50090-3958-0- Official label
- DailyMed (National Library of Medicine), updated Jun 16, 2021
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