Olanzapine 55111-0163
Product NDC
55111-0163- Manufacturer
- Dr. Reddy's Laboratories Ltd.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- April 23, 2012
- Listing Expires
- December 31, 2026
- Application
- ANDA076255
Need to source Olanzapine? Find it on a pharmacy-to-pharmacy marketplace at better prices.
✓ DSCSA Compliant. ✓ Verified Pharmacies Only.P2P pharmacy marketplace.
Active Ingredients
| Ingredient | Strength |
|---|---|
| Olanzapine | 2.5 mg/1 |
Drug Class
Atypical Antipsychotic [EPC]Atypical Antipsychotic [EPC]
Packaging Options(4)
100 TABLET, FILM COATED in 1 BOTTLE (55111-163-01)
500 TABLET, FILM COATED in 1 BOTTLE (55111-163-05)
30 TABLET, FILM COATED in 1 BOTTLE (55111-163-30)
10 BLISTER PACK in 1 CARTON (55111-163-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (55111-163-79)