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Amoxapine

NDC 62135-702, Amoxapine, tablet, from Chartwell RX, LLC.

Product NDC
62135-702
Status
Listed
Labeler
Chartwell RX, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA072879
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/62135-702 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • AMOXAPINE100 mg/1

Pharmacologic classes

Tricyclic Antidepressant [EPC]

Package NDCNDC-11Package
62135-702-906213507029090 TABLET in 1 BOTTLE (62135-702-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/eed5e856-dd7b-4eaa-9dad-508f2bef9328

Use it

Look up 62135-702 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/62135-702 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 62135-702. 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.