Nortriptyline Hydrochloride

Product NDC

68788-9879

11-digit product format

687889879

Labeler code

68788

Product ID

68788-9879_b6b0b34f-5bbd-4fc6-9941-b2c7f894d378

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Nortriptyline Hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc.

Application

ANDA074132

Marketing category

ANDA

Marketing start

2012-03-05

Marketing end

0000-00-00

Substance

NORTRIPTYLINE HYDROCHLORIDE

Active strength

50 mg/1

Pharmacologic classes

Tricyclic Antidepressant [EPC]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record