DURAGESIC

Product NDC
50458-105
11-digit product format
504580105
Labeler code
50458
Product ID
50458-105_d9a349c8-b6a3-11ec-bed1-85d730367705
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
fentanyl
Dosage form
PATCH
Route
TRANSDERMAL
Labeler
Janssen Pharmaceuticals, Inc.
Application
NDA019813
Marketing category
NDA
Marketing start
2018-11-05
Marketing end
2022-09-15
Substance
FENTANYL
Active strength
75 ug/1
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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50458-105-05EA - Each50458-10557d74f96-87f2-4602-8a48-00f473f1d6fe12019-04-11

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
50458-105-05504580105055 POUCH in 1 BOX (50458-105-05) > 1 PATCH in 1 POUCH5 pouch2018-11-150000-00-00NoNoCurrent