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DOXEPIN

NDC 59651-844, DOXEPIN, tablet, from Aurobindo Pharma Limited.

Product NDC
59651-844
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216041
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/59651-844 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DOXEPIN HYDROCHLORIDE3 mg/1

Pharmacologic classes

Tricyclic Antidepressant [EPC]

Package NDCNDC-11Package
59651-844-305965108443030 TABLET in 1 BOTTLE (59651-844-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/29b3bf98-2c57-4d87-b5eb-5232e46dc639

  • NADAC price for package 59651084430

    GET /v1/drugs/nadac/59651084430

Use it

Look up 59651-844 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/59651-844 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 59651-844. 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.