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DESIPRAMINE HYDROCHLORIDE

NDC 70518-4645, desipramine hydrochloride, tablet, from REMEDYREPACK INC..

Product NDC
70518-4645
Status
Listed
Labeler
REMEDYREPACK INC.
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/70518-4645 \
  -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
70518-4645-07051846450050 POUCH in 1 BOX (70518-4645-0) / 1 TABLET in 1 POUCH (70518-4645-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/dc1601be-e16a-411f-b9b8-01c51abb2441

Use it

Look up 70518-4645 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4645 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-4645. 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.