FDA.reportPublic FDA data

Clonidine Hydrochloride

Product NDC
68084-866
11-digit product format
680840866
Labeler code
68084
Product ID
68084-866_8647e5a3-ea2f-2b91-e053-2991aa0ae6dd
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Clonidine Hydrochloride
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
American Health Packaging
Application
ANDA202984
Marketing category
ANDA
Marketing start
2014-10-21
Marketing end
2020-06-30
Substance
CLONIDINE HYDROCHLORIDE
Active strength
0 mg/1
Pharmacologic classes
Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68084-866-11EA - Each68084-86690b9da05-2036-4f1b-baea-aac055191fb812014-12-01
68084-866-21EA - Each68084-8662592b22f-55d6-488b-8e3f-cb8cb5a9fb2a12014-12-01
68084-866-25EA - Each68084-86695040939-a8a3-4200-89b1-022893abad3a12016-03-04
68084-866-95EA - Each68084-8664ace30f5-3563-41f7-802b-41b96c32b15f12016-03-04