Linezolid
NDC 57664-683, linezolid, injection, solution, from Sun Pharmaceutical Industries, Inc..
- Product NDC
- 57664-683
- Status
- Listed
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA207354
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/57664-683 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- LINEZOLID600 mg/300mL
Pharmacologic classes
Oxazolidinone Antibacterial [EPC]; Oxazolidinones [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 57664-683-57 | 57664068357 | 10 BAG in 1 BOX (57664-683-57) / 300 mL in 1 BAG (57664-683-31) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/870c9600-04d5-4b44-a5b5-02252a310f22Medicare Part B payment limits (ASP)
GET /v1/drugs/asp?ndc=57664-683
Use it
Look up 57664-683 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/57664-683 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 57664-683. 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.