Clonidine

Product NDC
65038-041
11-digit product format
650380041
Labeler code
65038
Product ID
65038-041_44a7e257-1fe2-42bb-e054-00144ff8d46c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
CLONIDINE
Dosage form
PATCH, EXTENDED RELEASE
Route
TRANSDERMAL
Labeler
Corium International, Inc.
Application
ANDA079090
Marketing category
ANDA
Marketing start
2016-08-03
Marketing end
0000-00-00
Substance
CLONIDINE
Active strength
0 mg/24h
Pharmacologic classes
Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC]
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
65038-041-032021-07-19C16284748780-19d75b9d1-221a-f424-e053-dadaa90a57ce44a7e257-1fe1-42bb-e054-00144ff8d46c
65038-041-032020-01-31C16284748780-19d75b9d1-221a-f424-e053-dadaa90a57ce44a7e257-1fe1-42bb-e054-00144ff8d46c