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Mirtazapine

NDC 65862-001, Mirtazapine, tablet, film coated, from Aurobindo Pharma Limited.

Product NDC
65862-001
Status
Listed
Labeler
Aurobindo Pharma Limited
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/65862-001 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MIRTAZAPINE7.5 mg/1
Package NDCNDC-11Package
65862-001-0165862000101100 TABLET, FILM COATED in 1 BOTTLE (65862-001-01)
65862-001-0565862000105500 TABLET, FILM COATED in 1 BOTTLE (65862-001-05)
65862-001-306586200013030 TABLET, FILM COATED in 1 BOTTLE (65862-001-30)
65862-001-606586200016060 TABLET, FILM COATED in 1 BOTTLE (65862-001-60)
65862-001-906586200019090 TABLET, FILM COATED in 1 BOTTLE (65862-001-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a4c012f0-50b6-42fb-9f06-a14632f23f2e

Use it

Look up 65862-001 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65862-001 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65862-001. 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.