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DESIPRAMINE HYDROCHLORIDE

NDC 50742-112, desipramine hydrochloride, tablet, from Ingenus Pharmaceuticals, LLC.

Product NDC
50742-112
Status
Listed
Labeler
Ingenus Pharmaceuticals, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204963
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50742-112 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DESIPRAMINE HYDROCHLORIDE10 mg/1

Pharmacologic classes

Tricyclic Antidepressant [EPC]

Package NDCNDC-11Package
50742-112-0150742011201100 TABLET in 1 BOTTLE (50742-112-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/7280f157-3fff-41c5-b3f4-510b8bacdaba
  • NADAC price for package 50742011201

    GET /v1/drugs/nadac/50742011201

Use it

Look up 50742-112 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50742-112 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50742-112. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.