NDC 71335-2601 – Imipramine Hydrochloride

Imipramine Hydrochloride 25 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-2601

Product details

Brand name
Imipramine Hydrochloride
Generic name
Imipramine Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA040903
Marketed since
April 7, 2016
Listing expires
December 31, 2026
Pharmacologic class
Tricyclic Antidepressant

Active ingredients

Uses, dosage, side effects and warnings for Imipramine Hydrochloride →

Package NDC codes (3)

Package NDCDescriptionSince
71335-2601-130 TABLET, FILM COATED in 1 BOTTLE (71335-2601-1)Jun 5, 2025
71335-2601-260 TABLET, FILM COATED in 1 BOTTLE (71335-2601-2)Jun 5, 2025
71335-2601-390 TABLET, FILM COATED in 1 BOTTLE (71335-2601-3)Jun 5, 2025

Other Imipramine Hydrochloride products