Imipramine Hydrochloride

Product NDC

54738-914

11-digit product format

547380914

Labeler code

54738

Product ID

54738-914_615a19f8-e9e0-4366-e053-2a91aa0adb4d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Imipramine Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Richmond Pharmaceuticals, 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