Mirtazapine
NDC 57664-499, Mirtazapine, tablet, from Sun Pharmaceutical Industries, Inc..
- Product NDC
- 57664-499
- Status
- Listed
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA076541
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/57664-499 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- MIRTAZAPINE15 mg/1
| Package NDC | NDC-11 | Package |
|---|---|---|
| 57664-499-18 | 57664049918 | 1000 TABLET in 1 BOTTLE (57664-499-18) |
| 57664-499-83 | 57664049983 | 30 TABLET in 1 BOTTLE (57664-499-83) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/f23631be-c7ae-46e9-b771-a70be17bc9f0NADAC price for package 57664049918
GET /v1/drugs/nadac/57664049918NADAC price for package 57664049983
GET /v1/drugs/nadac/57664049983
Use it
Look up 57664-499 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/57664-499 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 57664-499. 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.