FENTANYL TRANSDERMAL

Product NDC
63629-4771
11-digit product format
636294771
Labeler code
63629
Product ID
63629-4771_544c9c05-8005-4108-9b0d-aed316e13391
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
fentanyl transdermal
Dosage form
PATCH, EXTENDED RELEASE
Route
TRANSDERMAL
Labeler
Bryant Ranch Prepack
Application
ANDA077154
Marketing category
ANDA
Marketing start
2011-02-09
Marketing end
0000-00-00
Substance
FENTANYL
Active strength
50 ug/h
Pharmacologic classes
Full Opioid Agonists [MoA], Opioid Agonist [EPC]
DEA schedule
CII
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63629-4771-1636294771011 POUCH in 1 CARTON (63629-4771-1) > 1 PATCH in 1 POUCH > 72 h in 1 PATCH1 pouch2011-02-090000-00-00NoNoCurrent
63629-4771-2636294771022 POUCH in 1 CARTON (63629-4771-2) > 1 PATCH in 1 POUCH > 72 h in 1 PATCH2 pouch2011-02-090000-00-00NoNoCurrent
63629-4771-3636294771035 POUCH in 1 CARTON (63629-4771-3) > 1 PATCH in 1 POUCH > 72 h in 1 PATCH5 pouch2011-02-090000-00-00NoNoCurrent