clonidine hydrochloride

Product NDC
76420-066
11-digit product format
764200066
Labeler code
76420
Product ID
76420-066_b26a7261-c68e-834b-e053-2a95a90a1f7d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Clonidine Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Asclemed USA, Inc.
Application
ANDA091368
Marketing category
ANDA
Marketing start
2016-05-03
Substance
CLONIDINE HYDROCHLORIDE
Active strength
.1 mg/1
Pharmacologic classes
Adrenergic alpha2-Agonists [MoA], Central alpha-2 Adrenergic Agonist [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
W76I6XXF06CLONIDINE HYDROCHLORIDE4205-91-8CLONIDINE HYDROCHLORIDE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
76420-066-0176420006601100 TABLET in 1 BOTTLE (76420-066-01) 100 tablet2020-10-24NoNoHistorical
76420-066-207642000662020 TABLET in 1 BOTTLE (76420-066-20) 20 tablet2020-10-24NoNoHistorical
76420-066-307642000663030 TABLET in 1 BOTTLE (76420-066-30) 30 tablet2020-10-24NoNoHistorical
76420-066-607642000666060 TABLET in 1 BOTTLE (76420-066-60) 60 tablet2020-10-24NoNoHistorical
76420-066-907642000669090 TABLET in 1 BOTTLE (76420-066-90) 90 tablet2020-10-24NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
clonidine hydrochlorideAsclemed USA, Inc. | ASCLEMED USA INC. DBA ENOVACHEM2020-10-24HUMAN PRESCRIPTION DRUG LABEL1