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Doxepin

NDC 72603-222, Doxepin, tablet, film coated, from North Star Rx LLC.

Product NDC
72603-222
Status
Listed
Labeler
North Star Rx 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/72603-222 \
  -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
72603-222-017260302220130 TABLET, FILM COATED in 1 BOTTLE (72603-222-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/12edd5c6-c863-b83a-e063-6294a90a2f36

  • NADAC price for package 72603022201

    GET /v1/drugs/nadac/72603022201

Use it

Look up 72603-222 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72603-222 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72603-222. 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.