Doxepin Hydrochloride

Product NDC

70518-1488

11-digit product format

705181488

Labeler code

70518

Product ID

70518-1488_93c25d42-22fb-19e7-e053-2a95a90a21f3

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

doxepin hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA070791

Marketing category

ANDA

Marketing start

2018-10-06

Marketing end

0000-00-00

Substance

DOXEPIN HYDROCHLORIDE

Active strength

25 mg/1

Pharmacologic classes

Tricyclic Antidepressant [EPC]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record