DURAGESIC

Product NDC
50458-102
11-digit product format
504580102
Labeler code
50458
Product ID
50458-102_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
25 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
50458-102-05EA - Each50458-102c7779a0a-768a-4ca7-8972-df99d3d6ab1612018-11-06

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
50458-102-05504580102055 POUCH in 1 BOX (50458-102-05) > 1 PATCH in 1 POUCH5 pouch2018-11-050000-00-00NoNoCurrent