Olanzapine
- Product NDC
- 72603-156
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Olanzapine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NorthStar RxLLC
- Application
- ANDA202862
- Marketing category
- ANDA
- Substance
- OLANZAPINE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 72603-156-01 | 30 TABLET, FILM COATED in 1 BOTTLE (72603-156-01) | 2023-07-05 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Olanzapine | NorthStar RxLLC | Macleods Pharmaceuticals Limited | 2024-07-03 | Human Prescription Drug Label | 2 |