Acitretin

Product NDC

0115-1669

11-digit product format

001151669

Labeler code

0115

Product ID

0115-1669_0c72486f-de6b-46dd-a35b-0f8d7240361e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Acitretin

Dosage form

CAPSULE

Route

ORAL

Labeler

Impax Generics

Application

ANDA202552

Marketing category

ANDA

Marketing start

2016-01-04

Marketing end

2019-08-31

Substance

ACITRETIN

Active strength

25 mg/1

Pharmacologic classes

Retinoid [EPC],Retinoids [CS]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record