FENTANYL TRANSDERMAL

Product NDC
63629-4764
11-digit product format
636294764
Labeler code
63629
Product ID
63629-4764_0cab6e1c-bed6-4a8b-92ec-d887301223b5
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
100 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
63629-4764-1636294764011 POUCH in 1 CARTON (63629-4764-1) > 1 PATCH in 1 POUCH > 72 h in 1 PATCH1 pouch2011-02-090000-00-00NoNoCurrent
63629-4764-2636294764022 POUCH in 1 CARTON (63629-4764-2) > 1 PATCH in 1 POUCH > 72 h in 1 PATCH2 pouch2011-02-090000-00-00NoNoCurrent
63629-4764-3636294764035 POUCH in 1 CARTON (63629-4764-3) > 1 PATCH in 1 POUCH > 72 h in 1 PATCH5 pouch2011-02-090000-00-00NoNoCurrent