Olanzapine 72789-0341
Product NDC
72789-0341- Manufacturer
- Pd-Rx Pharmaceuticals, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 22, 2014
- Listing Expires
- December 31, 2026
- Application
- ANDA202862
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Olanzapine | 20 mg/1 |
Drug Class
Atypical Antipsychotic [EPC]Atypical Antipsychotic [EPC]
Packaging Options(1)
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-341-90)