Olanzapine 67877-0174
Product NDC
67877-0174- Manufacturer
- Ascend Laboratories, Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 1, 2012
- Listing Expires
- December 31, 2026
- Application
- ANDA202295
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Olanzapine | 7.5 mg/1 |
Drug Class
Atypical Antipsychotic [EPC]Atypical Antipsychotic [EPC]
Packaging Options(6)
100 TABLET in 1 BOTTLE (67877-174-01)
1000 TABLET in 1 BOTTLE (67877-174-10)
30 TABLET in 1 BOTTLE (67877-174-30)
7 TABLET in 1 BOTTLE (67877-174-32)
10 BLISTER PACK in 1 CARTON (67877-174-35) / 10 TABLET in 1 BLISTER PACK (67877-174-33)
3 BLISTER PACK in 1 CARTON (67877-174-85) / 10 TABLET in 1 BLISTER PACK (67877-174-33)