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Doxepin

NDC 72819-161, Doxepin, tablet, film coated, from Archis Pharma LLC.

Product NDC
72819-161
Status
Listed
Labeler
Archis Pharma LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202337
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72819-161 \
  -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
72819-161-037281901610330 TABLET, FILM COATED in 1 BOTTLE (72819-161-03)
72819-161-1072819016110100 TABLET, FILM COATED in 1 BOTTLE (72819-161-10)
72819-161-1172819016111500 TABLET, FILM COATED in 1 BOTTLE (72819-161-11)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e3eac8e4-224e-4b7b-81d3-071301f914fa

  • NADAC price for package 72819016103

    GET /v1/drugs/nadac/72819016103

Use it

Look up 72819-161 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72819-161 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72819-161. 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.