Doxepin Hydrochloride

Product NDC

70518-1525

11-digit product format

705181525

Labeler code

70518

Product ID

70518-1525_7813d8cb-28af-5ce3-e053-2991aa0a5595

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

doxepin hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA070791

Marketing category

ANDA

Marketing start

2018-10-12

Marketing end

0000-00-00

Substance

DOXEPIN 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