Olanzapine 70518-1582
Product NDC
70518-1582- Manufacturer
- Remedyrepack Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 24, 2018
- Listing Expires
- December 31, 2027
- Application
- ANDA076133
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Olanzapine | 20 mg/1 |
Drug Class
Atypical Antipsychotic [EPC]Atypical Antipsychotic [EPC]
Packaging Options(1)
30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1582-0)