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Doxepin Hydrochloride

NDC 51672-1404, Doxepin Hydrochloride, cream, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-1404
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
CREAM
Route
TOPICAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213919
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-1404 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DOXEPIN HYDROCHLORIDE50 mg/g

Pharmacologic classes

Tricyclic Antidepressant [EPC]

Package NDCNDC-11Package
51672-1404-2516721404021 TUBE in 1 CARTON (51672-1404-2) / 30 g in 1 TUBE
51672-1404-9516721404091 TUBE in 1 CARTON (51672-1404-9) / 45 g in 1 TUBE

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0d4bff5c-4e3d-459e-aba2-9c4c34b5ba7b

Use it

Look up 51672-1404 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-1404 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-1404. 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.