DURAGESIC

Product NDC
50458-093
11-digit product format
504580093
Labeler code
50458
Product ID
50458-093_4510e337-3d1f-4eab-907e-85e95dc7d5a0
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
fentanyl
Dosage form
PATCH
Route
TRANSDERMAL
Labeler
Janssen Pharmaceuticals, Inc.
Application
NDA019813
Marketing category
NDA
Marketing start
1990-08-07
Marketing end
2020-03-31
Substance
FENTANYL
Active strength
75 ug/h
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
50458-093-05EA - Each50458-09397ef0d6d-caac-48d7-b4a6-9be3a1e50fb612012-07-24