NDC 0093-5248
Olanzapine 20 mg tablet, orally disintegrating
On the label: Teva Pharmaceuticals USA, Inc..
Where it's made
This label doesn't name the factory that makes the drug. 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 Teva Pharmaceuticals USA, Inc. names for other drugs.
Product details
- Generic drug
- Olanzapine: every company that makes it
- Form
- tablet, orally disintegrating, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA077243
- On the market since
- Jan 24, 2012
- Package NDCs
0093-5248-190093-5248-65- Official label
- DailyMed (National Library of Medicine), updated Feb 27, 2026
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