Nortriptyline Hydrochloride

Product NDC

50436-6650

11-digit product format

504366650

Labeler code

50436

Product ID

50436-6650_399b99d2-1cb8-49de-8487-9d39cc3cf001

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Nortriptyline Hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

Unit Dose Services

Application

ANDA073554

Marketing category

ANDA

Marketing start

1992-07-01

Marketing end

0000-00-00

Substance

NORTRIPTYLINE HYDROCHLORIDE

Active strength

25 mg/1

Pharmacologic classes

Tricyclic Antidepressant [EPC]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record