Clonidine Hydrochloride

Product NDC
53808-0230
11-digit product format
538080230
Labeler code
53808
Product ID
53808-0230_462a1a82-eaa9-4676-9569-925f18fd30d2
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Clonidine Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
State of Florida DOH Central Pharmacy
Application
ANDA070317
Marketing category
ANDA
Marketing start
2009-07-01
Marketing end
0000-00-00
Substance
CLONIDINE HYDROCHLORIDE
Active strength
0 mg/1
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
53808-0230-12021-12-29C16284748780-1956f9ecf-d23f-621f-e053-dbdaa90a74ad08c223a7-248a-444f-87ba-0844045e2b17
53808-0230-12019-10-21C16284748780-1956f9ecf-d23f-621f-e053-dbdaa90a74ad08c223a7-248a-444f-87ba-0844045e2b17