Imipramine Hydrochloride

Product NDC

70518-0006

11-digit product format

705180006

Labeler code

70518

Product ID

70518-0006_9e5ea757-e8f5-50f5-e053-2995a90aa4d3

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Imipramine Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA040903

Marketing category

ANDA

Marketing start

2016-11-17

Marketing end

0000-00-00

Substance

IMIPRAMINE HYDROCHLORIDE

Active strength

25 mg/1

Pharmacologic classes

Tricyclic Antidepressant [EPC]

NDC exclude flag

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record