Olanzapine
- Product NDC
- 0615-8244
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Olanzapine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- Application
- ANDA202862
- Marketing category
- ANDA
- Substance
- OLANZAPINE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 0615-8244-05 | 15 TABLET, FILM COATED in 1 BLISTER PACK (0615-8244-05) | 2024-07-24 | | No | Historical |
| 0615-8244-39 | 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8244-39) | 2018-11-02 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Olanzapine | NCS HealthCare of KY, LLC dba Vangard Labs | 2025-03-03 | HUMAN PRESCRIPTION DRUG LABEL | 13 |