Olanzapine
- Product NDC
- 71335-2599
- 11-digit product format
- 713352599
- Labeler code
- 71335
- Product ID
- 71335-2599_2b67795f-346b-4d05-9089-b0dd16244e07
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Olanzapine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA090798
- Marketing category
- ANDA
- Marketing start
- 2012-04-23
- Substance
- OLANZAPINE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| N7U69T4SZR | OLANZAPINE | 132539-06-1 | OLANZAPINE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2599-1 | 71335259901 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-2599-1) | 2025-06-05 | No | No | Historical |
| 71335-2599-2 | 71335259902 | 15 TABLET, FILM COATED in 1 BOTTLE (71335-2599-2) | 2025-06-05 | No | No | Historical |
| 71335-2599-3 | 71335259903 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-2599-3) | 2025-06-05 | No | No | Historical |
| 71335-2599-4 | 71335259904 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-2599-4) | 2025-06-05 | No | No | Historical |
| 71335-2599-5 | 71335259905 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-2599-5) | 2025-06-05 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Olanzapine | Bryant Ranch Prepack | 2025-06-05 | HUMAN PRESCRIPTION DRUG LABEL | 1 |