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Desipramine Hydrochloride

NDC 69238-1057, Desipramine, tablet, film coated, from Amneal Pharmaceuticals LLC.

Product NDC
69238-1057
Status
Listed
Labeler
Amneal Pharmaceuticals LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208105
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69238-1057 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DESIPRAMINE HYDROCHLORIDE50 mg/1

Pharmacologic classes

Tricyclic Antidepressant [EPC]

Package NDCNDC-11Package
69238-1057-169238105701100 TABLET, FILM COATED in 1 BOTTLE (69238-1057-1)
69238-1057-36923810570330 TABLET, FILM COATED in 1 BOTTLE (69238-1057-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a3b4b25d-0ddb-4531-badb-f1ba3168ac07

  • NADAC price for package 69238105701

    GET /v1/drugs/nadac/69238105701

Use it

Look up 69238-1057 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69238-1057 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69238-1057. 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.