Olanzapine 43598-0166
Product NDC
43598-0166- Manufacturer
- Dr. Reddy's Laboratories Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 10, 2013
- Listing Expires
- December 31, 2026
- Application
- ANDA076255
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Olanzapine | 10 mg/1 |
Drug Class
Atypical Antipsychotic [EPC]Atypical Antipsychotic [EPC]
Packaging Options(6)
100 TABLET, FILM COATED in 1 BOTTLE (43598-166-01)
500 TABLET, FILM COATED in 1 BOTTLE (43598-166-05)
1000 TABLET, FILM COATED in 1 BOTTLE (43598-166-10)
30 TABLET, FILM COATED in 1 BOTTLE (43598-166-30)
60 TABLET, FILM COATED in 1 BOTTLE (43598-166-60)
10 BLISTER PACK in 1 CARTON (43598-166-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (43598-166-79)