United States · FDA National Drug Code directory

Imipramine 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: 71205-804_3f90b8dd-7234-4428-b896-943d052dd05f
Product NDC: 71205-804
Form: TABLET, FILM COATED
Composition / generic term: Imipramine Hydrochloride
Labeler: Proficient Rx LP
Marketing category: ANDA
Marketing start / end (source format): 20160407
Source listing expiry: 20261231

Source-listed ingredients

IMIPRAMINE HYDROCHLORIDE — 10 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

30 TABLET, FILM COATED in 1 BOTTLE (71205-804-30) · 71205-804-30
60 TABLET, FILM COATED in 1 BOTTLE (71205-804-60) · 71205-804-60
90 TABLET, FILM COATED in 1 BOTTLE (71205-804-90) · 71205-804-90

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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