Fentanyl

Product NDC

49999-831

11-digit product format

499990831

Labeler code

49999

Product ID

49999-831_f9fc2d3e-3f70-459a-8a22-588bd6dd2443

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Fentanyl

Dosage form

PATCH, EXTENDED RELEASE

Route

TRANSDERMAL

Labeler

Lake Erie Medical DBA Quality Care Products LLC

Application

ANDA076709

Marketing category

ANDA

Marketing start

2011-12-09

Marketing end

0000-00-00

Substance

FENTANYL

Active strength

25 ug/72h

Pharmacologic classes

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

DEA schedule

CII

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record