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Imipramine Hydrochloride

NDC 69315-134, Imipramine Hydrochloride, tablet, film coated, from Leading Pharma, LLC.

Product NDC
69315-134
Status
Listed
Labeler
Leading Pharma, LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA040903
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69315-134 \
  -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
69315-134-0169315013401100 TABLET, FILM COATED in 1 BOTTLE (69315-134-01)
69315-134-10693150134101000 TABLET, FILM COATED in 1 BOTTLE (69315-134-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/490263ce-b4d2-428a-87da-fcd07f85499a

  • NADAC price for package 69315013401

    GET /v1/drugs/nadac/69315013401

  • NADAC price for package 69315013410

    GET /v1/drugs/nadac/69315013410

Use it

Look up 69315-134 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69315-134 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69315-134. 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.