Nortriptyline Hydrochloride

Product NDC

49999-215

11-digit product format

499990215

Labeler code

49999

Product ID

49999-215_fbe88b7c-9ce3-4bfd-ba53-e9b7c8b6a3b5

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Nortriptyline Hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

Lake Erie Medical DBA Quality Care Products LLC

Application

ANDA074132

Marketing category

ANDA

Marketing start

2011-01-27

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