Fentanyl

Product NDC

35356-062

11-digit product format

353560062

Labeler code

35356

Product ID

35356-062_b828062d-b4b9-4395-98cb-077f85397581

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

fentanyl

Dosage form

PATCH

Route

TRANSDERMAL

Labeler

Lake Erie Medical DBA Quality Care Products LLC

Application

ANDA076258

Marketing category

ANDA

Marketing start

2013-01-09

Marketing end

0000-00-00

Substance

FENTANYL

Active strength

12 ug/h

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