Fentanyl

Product NDC
35356-635
11-digit product format
353560635
Labeler code
35356
Product ID
35356-635_08eb59cb-7b91-4114-aba3-d10a4b194330
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
fentanyl
Dosage form
PATCH
Route
TRANSDERMAL
Labeler
Lake Erie Medical DBA Quality Care Products LLC
Application
ANDA076258
Marketing category
ANDA
Marketing start
2013-01-09
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
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
35356-635-05EA - Each35356-635d77c70a3-c836-4ce1-8b14-397e46167c1912014-09-03