Doxepin Hydrochloride

Product NDC

40085-716

11-digit product format

400850716

Labeler code

40085

Product ID

40085-716_8989ba3a-9624-40f6-92d4-7ec21d75e54d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Doxepin Hydrochloride

Dosage form

CREAM

Route

TOPICAL

Labeler

Renaissance Pharma, Inc.

Application

NDA020126

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2016-03-07

Marketing end

2019-12-31

Substance

DOXEPIN HYDROCHLORIDE

Active strength

50 mg/g

Pharmacologic classes

Tricyclic Antidepressant [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record