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Active ingredient

Imipramine

40 finished FDA listings contain Imipramine as their only active ingredient.

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FDA NDC Directory

Ingredient names as written by FDA
IMIPRAMINE HYDROCHLORIDE, IMIPRAMINE PAMOATE
Dosage forms
Capsule, Tablet, Tablet, Film Coated
Routes
Oral
Manufacturers / labelers
14
Strengths listed
10 mg/1 · 100 mg/1 · 125 mg/1 · 150 mg/1 · 25 mg/1 · 50 mg/1 · 75 mg/1

RxNorm (National Library of Medicine)

Ingredient concept RxCUI 5691

Drugs@FDA applications

Linked only where the FDA listing’s application number matches Drugs@FDA exactly. A listing in the NDC Directory does not by itself mean FDA approval.

ApplicationSponsorOriginal approvalListings
ANDA 088262STRIDES PHARMA INTL1983-10-211
ANDA 088292STRIDES PHARMA INTL1983-10-211
ANDA 088276STRIDES PHARMA INTL1983-10-211
ANDA 040751OXFORD PHARMS2008-02-2813
ANDA 090441CHARTWELL2010-03-111
ANDA 091099HIKMA2010-04-164
ANDA 090444LUPIN LTD2010-04-165
ANDA 040903LEADING2012-10-2412

Official labeling on DailyMed

Showing the 12 most recent of 20 labels.

Sources: FDA NDC Directory (2026-09-29), RxNorm, Drugs@FDA, DailyMed. Each source’s facts are shown separately as published.