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Doxepin Hydrochloride

NDC 71921-164, Doxepin Hydrochloride, capsule, from Florida Pharmaceutical Products, LLC.

Product NDC
71921-164
Status
Listed
Labeler
Florida Pharmaceutical Products, LLC
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213474
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71921-164 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DOXEPIN HYDROCHLORIDE50 mg/1

Pharmacologic classes

Tricyclic Antidepressant [EPC]

Package NDCNDC-11Package
71921-164-0171921016401100 CAPSULE in 1 BOTTLE (71921-164-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b787a283-f882-e1f0-e053-2a95a90a8975

Use it

Look up 71921-164 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71921-164 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71921-164. 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.