Nortriptyline Hydrochloride

Product NDC

0179-0223

11-digit product format

001790223

Labeler code

0179

Product ID

0179-0223_7b34fae3-1ad3-4c8f-e053-2a91aa0a3430

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Nortriptyline Hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

KAISER FOUNDATION HOSPITA

Application

ANDA073553

Marketing category

ANDA

Marketing start

2017-01-17

Marketing end

2019-03-31

Substance

NORTRIPTYLINE H

Active strength

10 mg/1

Pharmacologic classes

Tricyclic Antid

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record