NDC 71335-2266 – Clonidine hydrochloride

Clonidine Hydrochloride .1 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2266

Product details

Brand name
Clonidine hydrochloride
Generic name
Clonidine hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078895
Marketed since
December 24, 2020
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
71335-2266-024 TABLET in 1 BOTTLE, PLASTIC (71335-2266-0)Nov 30, 2023
71335-2266-1100 TABLET in 1 BOTTLE, PLASTIC (71335-2266-1)Nov 30, 2023
71335-2266-230 TABLET in 1 BOTTLE, PLASTIC (71335-2266-2)Nov 30, 2023
71335-2266-320 TABLET in 1 BOTTLE, PLASTIC (71335-2266-3)Nov 30, 2023
71335-2266-460 TABLET in 1 BOTTLE, PLASTIC (71335-2266-4)Nov 30, 2023
71335-2266-5120 TABLET in 1 BOTTLE, PLASTIC (71335-2266-5)Nov 30, 2023
71335-2266-690 TABLET in 1 BOTTLE, PLASTIC (71335-2266-6)Nov 30, 2023
71335-2266-710 TABLET in 1 BOTTLE, PLASTIC (71335-2266-7)Nov 30, 2023
71335-2266-845 TABLET in 1 BOTTLE, PLASTIC (71335-2266-8)Nov 30, 2023
71335-2266-914 TABLET in 1 BOTTLE, PLASTIC (71335-2266-9)Nov 30, 2023

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