Desipramine Hydrochloride

Product NDC

64720-417

11-digit product format

647200417

Labeler code

64720

Product ID

64720-417_44fdecf5-ad29-4abc-a7f9-7a5e7e4f0f9b

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Desipramine Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

CorePharma, LLC

Application

ANDA205153

Marketing category

ANDA

Marketing start

2017-07-14

Marketing end

2019-09-30

Substance

DESIPRAMINE 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