Fentanyl

Product NDC

0591-3213

11-digit product format

005913213

Labeler code

0591

Product ID

0591-3213_89a9c234-ef0a-4c40-8473-3ccd17c9640b

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Fentanyl

Dosage form

PATCH, EXTENDED RELEASE

Route

TRANSDERMAL

Labeler

Actavis Pharma, Inc.

Application

ANDA076709

Marketing category

ANDA

Marketing start

2007-08-21

Marketing end

2019-08-31

Substance

FENTANYL

Active strength

75 ug/h

Pharmacologic classes

Full Opioid Agonists [MoA],Opioid Agonist [EPC]

DEA schedule

CII

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record