Desipramine Hydrochloride

Product NDC

0781-5218

11-digit product format

007815218

Labeler code

0781

Product ID

0781-5218_69485d1b-0164-4d9b-b3b9-9b29304ab311

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Desipramine Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Sandoz Inc

Application

ANDA072099

Marketing category

ANDA

Marketing start

1988-05-24

Marketing end

2020-06-30

Substance

DESIPRAMINE HYDROCHLORIDE

Active strength

10 mg/1

Pharmacologic classes

Tricyclic Antidepressant [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record