NDC 71335-0777 – clonidine hydrochloride

Clonidine Hydrochloride .1 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0777

Product details

Brand name
clonidine hydrochloride
Generic name
Clonidine Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA091368
Marketed since
May 3, 2016
Listing expires
December 31, 2026
Pharmacologic class
Central alpha-2 Adrenergic Agonist

Active ingredients

Uses, dosage, side effects and warnings for Clonidine Hydrochloride →

Package NDC codes (10)

Package NDCDescriptionSince
71335-0777-024 TABLET in 1 BOTTLE (71335-0777-0)Dec 27, 2021
71335-0777-1100 TABLET in 1 BOTTLE (71335-0777-1)Apr 27, 2018
71335-0777-230 TABLET in 1 BOTTLE (71335-0777-2)Apr 16, 2018
71335-0777-320 TABLET in 1 BOTTLE (71335-0777-3)Apr 21, 2021
71335-0777-460 TABLET in 1 BOTTLE (71335-0777-4)Jul 30, 2018
71335-0777-5120 TABLET in 1 BOTTLE (71335-0777-5)Apr 12, 2018
71335-0777-690 TABLET in 1 BOTTLE (71335-0777-6)Apr 20, 2018
71335-0777-710 TABLET in 1 BOTTLE (71335-0777-7)Apr 13, 2021
71335-0777-845 TABLET in 1 BOTTLE (71335-0777-8)Dec 27, 2021
71335-0777-914 TABLET in 1 BOTTLE (71335-0777-9)Jan 26, 2021

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