Olanzapine 33342-0072
Product NDC
33342-0072- Manufacturer
- Macleods Pharmaceuticals Limited
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 22, 2014
- Listing Expires
- December 31, 2027
- Application
- ANDA202862
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Olanzapine | 20 mg/1 |
Drug Class
Atypical Antipsychotic [EPC]Atypical Antipsychotic [EPC]
Packaging Options(5)
30 TABLET, FILM COATED in 1 BOTTLE (33342-072-07)
100 TABLET, FILM COATED in 1 BOTTLE (33342-072-11)
10 BLISTER PACK in 1 CARTON (33342-072-12) / 10 TABLET, FILM COATED in 1 BLISTER PACK
500 TABLET, FILM COATED in 1 BOTTLE (33342-072-15)
1000 TABLET, FILM COATED in 1 BOTTLE (33342-072-44)