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Trazodone Hydrochloride

NDC 69584-885, Trazodone Hydrochloride, tablet, film coated, from Oxford Pharmaceuticals, LLC.

Product NDC
69584-885
Status
Listed
Labeler
Oxford Pharmaceuticals, LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA072193
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69584-885 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TRAZODONE HYDROCHLORIDE100 mg/1

Pharmacologic classes

Serotonin Reuptake Inhibitor [EPC]

Package NDCNDC-11Package
69584-885-096958408850990 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69584-885-09)
69584-885-1069584088510100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69584-885-10)
69584-885-5069584088550500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69584-885-50)
69584-885-90695840885901000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69584-885-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/283c8236-9776-44cb-b7b2-1024689de736

Use it

Look up 69584-885 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69584-885 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69584-885. 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.