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Imipramine Hydrochloride

NDC 70868-810, Imipramine Hydrochloride, tablet, film coated, from Key Therapeutics.

Product NDC
70868-810
Status
Listed
Labeler
Key Therapeutics
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA040751
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70868-810 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • IMIPRAMINE HYDROCHLORIDE25 mg/1

Pharmacologic classes

Tricyclic Antidepressant [EPC]

Package NDCNDC-11Package
70868-810-1070868081010100 TABLET, FILM COATED in 1 BOTTLE (70868-810-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/9c685c94-64cd-442a-ade7-193c62d7a058

Use it

Look up 70868-810 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70868-810 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70868-810. 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.