Fentanyl

Product NDC

0781-7242

11-digit product format

007817242

Labeler code

0781

Product ID

0781-7242_5599f15f-4618-4b48-856e-83db0dccd957

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Fentanyl

Dosage form

PATCH

Route

TRANSDERMAL

Labeler

Sandoz,Inc.

Application

NDA019813

Marketing category

NDA

Marketing start

2004-10-01

Marketing end

0000-00-00

Substance

FENTANYL

Active strength

50 ug/h

Pharmacologic classes

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

DEA schedule

CII

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record