Desipramine Hydrochloride

Product NDC

0781-1976

11-digit product format

007811976

Labeler code

0781

Product ID

0781-1976_69485d1b-0164-4d9b-b3b9-9b29304ab311

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Desipramine Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Sandoz Inc

Application

ANDA072104

Marketing category

ANDA

Marketing start

1988-06-20

Marketing end

2019-12-31

Substance

DESIPRAMINE HYDROCHLORIDE

Active strength

150 mg/1

Pharmacologic classes

Tricyclic Antidepressant [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record