Olanzapine 72189-0578
Product NDC
72189-0578- Manufacturer
- Direct_rx
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 17, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA202862
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Olanzapine | 7.5 mg/1 |
Drug Class
Atypical Antipsychotic [EPC]Atypical Antipsychotic [EPC]
Packaging Options(1)
30 TABLET, FILM COATED in 1 BOTTLE (72189-578-30)