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Linezolid

NDC 57664-682, linezolid, injection, solution, from Sun Pharmaceutical Industries, Inc..

Product NDC
57664-682
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
Request
curl https://api.healthcare.dev/v1/drugs/ndc/57664-682 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LINEZOLID200 mg/100mL

Pharmacologic classes

Oxazolidinone Antibacterial [EPC]; Oxazolidinones [CS]

Package NDCNDC-11Package
57664-682-3057664068230100 mL in 1 BAG (57664-682-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/870c9600-04d5-4b44-a5b5-02252a310f22

Use it

Look up 57664-682 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/57664-682 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 57664-682. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.