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Mirtazapine

NDC 57664-500, Mirtazapine, tablet, from Sun Pharmaceutical Industries, Inc..

Product NDC
57664-500
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
Request
curl https://api.healthcare.dev/v1/drugs/ndc/57664-500 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MIRTAZAPINE30 mg/1
Package NDCNDC-11Package
57664-500-18576640500181000 TABLET in 1 BOTTLE (57664-500-18)
57664-500-835766405008330 TABLET in 1 BOTTLE (57664-500-83)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f23631be-c7ae-46e9-b771-a70be17bc9f0

  • NADAC price for package 57664050083

    GET /v1/drugs/nadac/57664050083

Use it

Look up 57664-500 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/57664-500 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 57664-500. 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.