Olanzapine
NDC 68084-529, Olanzapine, tablet, film coated, from American Health Packaging.
- Product NDC
- 68084-529
- Status
- Listed
- Labeler
- American Health Packaging
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA076133
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/68084-529 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- OLANZAPINE20 mg/1
Pharmacologic classes
Atypical Antipsychotic [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 68084-529-01 | 68084052901 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-529-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-529-11) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/c0d705bf-b719-4c7b-b83d-c17d41cbbfadNADAC price for package 68084052901
GET /v1/drugs/nadac/68084052901
Use it
Look up 68084-529 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/68084-529 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 68084-529. 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.