Mirtazapine
NDC 67046-0068, Mirtazapine, tablet, film coated, from Coupler LLC.
- Product NDC
- 67046-0068
- Status
- Listed
- Labeler
- Coupler LLC
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA076921
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/67046-0068 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- MIRTAZAPINE30 mg/1
| Package NDC | NDC-11 | Package |
|---|---|---|
| 67046-0068-3 | 67046006803 | 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-0068-3) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/50718832-88fb-dec1-e063-6294a90ae468
Use it
Look up 67046-0068 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/67046-0068 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 67046-0068. 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.