Clonidine Hydrochloride

Product NDC
59746-668
11-digit product format
597460668
Labeler code
59746
Product ID
59746-668_05db5df2-4559-4fb1-a332-568878872d0f
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
clonidine hydrochloride
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
Jubilant Cadista Pharmaceuticals Inc.
Application
ANDA210338
Marketing category
ANDA
Marketing start
2018-01-29
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
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59746-668CLONIDINE HYDROCHLORIDE TABLET, EXTENDED RELEASE [JUBILANT CADISTA PHARMACEUTICALS INC.]3Legacy NDC20180223_d264c690-c017-844f-32ad-8335580d3aef.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
59746-668-0159746066801100 TABLET, EXTENDED RELEASE in 1 BOTTLE (59746-668-01) 2018-01-290000-00-00NoNoCurrent
59746-668-10597460668101000 TABLET, EXTENDED RELEASE in 1 BOTTLE (59746-668-10) 2018-01-290000-00-00NoNoCurrent
59746-668-305974606683030 TABLET, EXTENDED RELEASE in 1 BOTTLE (59746-668-30) 2018-01-290000-00-00NoNoCurrent
59746-668-605974606686060 TABLET, EXTENDED RELEASE in 1 BOTTLE (59746-668-60) 2018-01-290000-00-00NoNoCurrent