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Imipramine Hydrochloride

NDC 70518-3526, Imipramine Hydrochloride, tablet, from REMEDYREPACK INC..

Product NDC
70518-3526
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA040751
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3526 \
  -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
70518-3526-07051835260030 TABLET in 1 BLISTER PACK (70518-3526-0)
70518-3526-170518352601100 POUCH in 1 BOX (70518-3526-1) / 1 TABLET in 1 POUCH (70518-3526-2)
70518-3526-37051835260350 POUCH in 1 BOX (70518-3526-3) / 1 TABLET in 1 POUCH (70518-3526-2)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/02c19a0a-3d9d-4881-ad14-1687aafd87b5

Use it

Look up 70518-3526 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3526 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-3526. 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.