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Amoxapine

NDC 0591-5714, Amoxapine, tablet, from Actavis Pharma, Inc..

Product NDC
0591-5714
Status
Listed
Labeler
Actavis Pharma, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA072691
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0591-5714 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • AMOXAPINE50 mg/1

Pharmacologic classes

Tricyclic Antidepressant [EPC]

Package NDCNDC-11Package
0591-5714-0100591571401100 TABLET in 1 BOTTLE, PLASTIC (0591-5714-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a16297df-3158-48db-85e5-5cd506885556

Use it

Look up 0591-5714 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0591-5714 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0591-5714. 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.