Olanzapine 00781-3159
Product NDC
00781-3159- Manufacturer
- Sandoz Inc
- Dosage Form
- Injection, Powder, For Solution
- Route
- Intramuscular
- Product Type
- Human Prescription Drug
- Marketing Start
- October 24, 2011
- Listing Expires
- December 31, 2027
- Application
- ANDA201588
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Olanzapine | 10 mg/2mL |
Drug Class
Atypical Antipsychotic [EPC]Atypical Antipsychotic [EPC]
Packaging Options(1)
1 VIAL in 1 CARTON (0781-3159-72) / 2 mL in 1 VIAL