Imipramine Hydrochloride

Product NDC

53489-332

11-digit product format

534890332

Labeler code

53489

Product ID

53489-332_9e0586d7-3835-4ee5-9bff-141344f3e611

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Imipramine Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Sun Pharmaceutical Industries, Inc.

Application

ANDA081050

Marketing category

ANDA

Marketing start

1990-06-05

Marketing end

2020-12-31

Substance

IMIPRAMINE HYDROCHLORIDE

Active strength

50 mg/1

Pharmacologic classes

Tricyclic Antidepressant [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record