NDC 71205-804 – Imipramine Hydrochloride

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

Human Prescription Drug

Product NDC71205-804

Product details

Brand name
Imipramine Hydrochloride
Generic name
Imipramine Hydrochloride
Labeler
Proficient Rx LP
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
71205-804-3030 TABLET, FILM COATED in 1 BOTTLE (71205-804-30)Jun 5, 2023
71205-804-6060 TABLET, FILM COATED in 1 BOTTLE (71205-804-60)Jun 5, 2023
71205-804-9090 TABLET, FILM COATED in 1 BOTTLE (71205-804-90)Jun 5, 2023

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