Olanzapine
NDC 71610-419, Olanzapine, tablet, film coated, from Aphena Pharma Solutions - Tennessee, LLC.
- Product NDC
- 71610-419
- Status
- Listed
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA090798
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71610-419 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- OLANZAPINE15 mg/1
Pharmacologic classes
Atypical Antipsychotic [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 71610-419-30 | 71610041930 | 30 TABLET, FILM COATED in 1 BOTTLE (71610-419-30) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/b6ec5610-b4a6-4646-954a-0fe8b1d3e143
Use it
Look up 71610-419 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71610-419 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71610-419. 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.