mirtazapine
NDC 72865-371, mirtazapine, tablet, film coated, from XLCare Pharmaceuticals Inc..
- Product NDC
- 72865-371
- Status
- Listed
- Labeler
- XLCare Pharmaceuticals Inc.
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA219721
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/72865-371 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- MIRTAZAPINE45 mg/1
| Package NDC | NDC-11 | Package |
|---|---|---|
| 72865-371-05 | 72865037105 | 500 TABLET, FILM COATED in 1 BOTTLE (72865-371-05) |
| 72865-371-30 | 72865037130 | 30 TABLET, FILM COATED in 1 BOTTLE (72865-371-30) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/b6b31703-e77d-4d1a-b1ac-da972117e356
Use it
Look up 72865-371 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/72865-371 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 72865-371. 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.