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Mirtazapine

NDC 63739-099, Mirtazapine, tablet, film coated, from McKesson Corporation dba SKY Packaging.

Product NDC
63739-099
Status
Listed
Labeler
McKesson Corporation dba SKY Packaging
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077666
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/63739-099 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MIRTAZAPINE30 mg/1
Package NDCNDC-11Package
63739-099-106373900991010 BLISTER PACK in 1 BOX (63739-099-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/40c95daa-bbd5-48d9-97e4-c87f2c1f0fa5

Use it

Look up 63739-099 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63739-099 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63739-099. 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.