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mirtazapine

NDC 72865-368, mirtazapine, tablet, film coated, from XLCare Pharmaceuticals Inc..

Product NDC
72865-368
Status
Listed
Labeler
XLCare Pharmaceuticals Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA219721
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72865-368 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MIRTAZAPINE7.5 mg/1
Package NDCNDC-11Package
72865-368-0572865036805500 TABLET, FILM COATED in 1 BOTTLE (72865-368-05)
72865-368-307286503683030 TABLET, FILM COATED in 1 BOTTLE (72865-368-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b6b31703-e77d-4d1a-b1ac-da972117e356

Use it

Look up 72865-368 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72865-368 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72865-368. 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.