United States · FDA National Drug Code directory

Desipramine Hydrochloride

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference: 45963-342_b7478143-a6d3-4a43-ba49-63a8b422fa50
Product NDC: 45963-342
Form: TABLET, FILM COATED
Composition / generic term: Desipramine Hydrochloride
Labeler: Actavis Pharma, Inc.
Marketing category: ANDA
Marketing start / end (source format): 20060501 / 20270731

Source-listed ingredients

DESIPRAMINE HYDROCHLORIDE — 25 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

100 TABLET, FILM COATED in 1 BOTTLE (45963-342-02) · 45963-342-02

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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