Nortriptyline Hydrochloride

Product NDC

50436-0810

11-digit product format

504360810

Labeler code

50436

Product ID

50436-0810_6e7cbe57-a125-442b-ae84-6f02bfa5e124

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Nortriptyline Hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

Unit Dose Services

Application

ANDA074132

Marketing category

ANDA

Marketing start

1995-04-05

Marketing end

0000-00-00

Substance

NORTRIPTYLINE HYDROCHLORIDE

Active strength

10 mg/1

Pharmacologic classes

Tricyclic Antidepressant [EPC]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record