NDC 71335-3106 – Imipramine Hydrochloride

Imipramine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-3106

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, 2027
Pharmacologic class
Tricyclic Antidepressant

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
71335-3106-130 TABLET, FILM COATED in 1 BOTTLE (71335-3106-1)Mar 16, 2026
71335-3106-2100 TABLET, FILM COATED in 1 BOTTLE (71335-3106-2)Mar 16, 2026

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