Doxepin Hydrochloride

Product NDC

55289-018

11-digit product format

552890018

Labeler code

55289

Product ID

55289-018_7bd5c1e5-3c4f-7925-e053-2991aa0af5f4

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

doxepin hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

PD-Rx Pharmaceuticals, Inc.

Application

ANDA070791

Marketing category

ANDA

Marketing start

1986-05-13

Marketing end

0000-00-00

Substance

DOXEPIN HYDROCHLORIDE

Active strength

50 mg/1

Pharmacologic classes

Tricyclic Antidepressant [EPC]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record