Desipramine Hydrochloride

Product NDC

62559-714

11-digit product format

625590714

Labeler code

62559

Product ID

62559-714_9528b991-b4bc-4f30-a41e-d1b99aa8b5f6

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Desipramine Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

ANI Pharmaceuticals, Inc.

Application

ANDA205153

Marketing category

ANDA

Marketing start

2019-01-22

Marketing end

2020-12-31

Substance

DESIPRAMINE HYDROCHLORIDE

Active strength

100 mg/1

Pharmacologic classes

Tricyclic Antidepressant [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record