Olanzapine
NDC 68788-4012, Olanzapine, tablet, film coated, from Preferred Pharmaceuticals Inc..
- Product NDC
- 68788-4012
- Status
- Listed
- Labeler
- Preferred Pharmaceuticals Inc.
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA076255
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/68788-4012 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- OLANZAPINE2.5 mg/1
Pharmacologic classes
Atypical Antipsychotic [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 68788-4012-3 | 68788401203 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-4012-3) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/cfc0f187-d3ff-4bbb-9129-0e94c6eda0ee
Use it
Look up 68788-4012 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/68788-4012 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 68788-4012. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.