Doxepin Hydrochloride

Product NDC

70518-0865

11-digit product format

705180865

Labeler code

70518

Product ID

70518-0865_8e64f8fc-ebfb-0ae0-e053-2a95a90ae867

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Doxepin Hydrochloride

Dosage form

CREAM

Route

TOPICAL

Labeler

REMEDYREPACK INC.

Application

NDA020126

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2017-11-24

Marketing end

0000-00-00

Substance

DOXEPIN HYDROCHLORIDE

Active strength

50 mg/g

Pharmacologic classes

Tricyclic Antidepressant [EPC]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record