NDC 23155-580

Desipramine Hydrochloride 50 mg tablet

On the label: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc..

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
USV Private LimitedDaman, IndiaMakes it, tests it, packages it and labels it Serious problems, FDA actionApr 17, 2026 · 8 inspections, 3 with FDA action

Recalls

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug
Desipramine: every company that makes it
Form
tablet
Strength
50 mg
Approval
ANDA ANDA207433
On the market since
Nov 1, 2016
Package NDCs
23155-580-01
Official label
DailyMed (National Library of Medicine), updated Aug 26, 2025

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