clonidine hydrochloride

Product NDC
71205-570
11-digit product format
712050570
Labeler code
71205
Product ID
71205-570_cabfb3a4-d7d5-4211-b5f7-a89b5f988133
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
clonidine hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Proficient Rx LP
Application
ANDA078895
Marketing category
ANDA
Marketing start
2020-12-24
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
71205-570-127120505701212 TABLET in 1 BOTTLE, PLASTIC (71205-570-12) 12 tablet2021-05-26NoNoHistorical
71205-570-207120505702020 TABLET in 1 BOTTLE, PLASTIC (71205-570-20) 20 tablet2021-05-26NoNoHistorical
71205-570-307120505703030 TABLET in 1 BOTTLE, PLASTIC (71205-570-30) 30 tablet2021-05-26NoNoHistorical
71205-570-607120505706060 TABLET in 1 BOTTLE, PLASTIC (71205-570-60) 60 tablet2021-05-26NoNoHistorical
71205-570-907120505709090 TABLET in 1 BOTTLE, PLASTIC (71205-570-90) 90 tablet2021-05-26NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Clonidine Hydrochloride Tablets, USPProficient Rx LP2022-08-01HUMAN PRESCRIPTION DRUG LABEL2