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Mirtazapine

NDC 17856-0101, Mirtazapine, tablet, film coated, from ATLANTIC BIOLOGICALS CORP..

Product NDC
17856-0101
Status
Listed
Labeler
ATLANTIC BIOLOGICALS CORP.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076921
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/17856-0101 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MIRTAZAPINE7.5 mg/1
Package NDCNDC-11Package
17856-0101-117856010101100 POUCH in 1 BOX, UNIT-DOSE (17856-0101-1) / 1 TABLET, FILM COATED in 1 POUCH

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e6e5cbf7-a958-4ef8-abcc-a7491edb9520

Use it

Look up 17856-0101 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/17856-0101 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 17856-0101. 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.