NDC 0121-1072
OlanzapineIntramuscular 10 mg per 2 mL injection, powder, for solution
On the label: Pharmaceutical Associates, 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 Pharmaceutical Associates, Inc. names for other drugs.
Product details
- Generic drug
- Olanzapine: every company that makes it
- Form
- injection, powder, for solution, intramuscular
- Strength
- 10 mg per 2 mL
- Approval
- ANDA ANDA211072
- On the market since
- Jul 25, 2025
- Package NDCs
0121-1072-55- Official label
- DailyMed (National Library of Medicine), updated Jun 30, 2025
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