NDC 71335-2489 – Clonidine Hydrochloride

Clonidine Hydrochloride .1 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2489

Product details

Brand name
Clonidine Hydrochloride
Generic name
Clonidine Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA202297
Marketed since
July 1, 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
71335-2489-024 TABLET in 1 BOTTLE (71335-2489-0)Sep 18, 2024
71335-2489-1100 TABLET in 1 BOTTLE (71335-2489-1)Sep 18, 2024
71335-2489-230 TABLET in 1 BOTTLE (71335-2489-2)Sep 18, 2024
71335-2489-320 TABLET in 1 BOTTLE (71335-2489-3)Sep 18, 2024
71335-2489-460 TABLET in 1 BOTTLE (71335-2489-4)Sep 18, 2024
71335-2489-5120 TABLET in 1 BOTTLE (71335-2489-5)Sep 18, 2024
71335-2489-690 TABLET in 1 BOTTLE (71335-2489-6)Sep 18, 2024
71335-2489-710 TABLET in 1 BOTTLE (71335-2489-7)Sep 18, 2024
71335-2489-845 TABLET in 1 BOTTLE (71335-2489-8)Sep 18, 2024
71335-2489-914 TABLET in 1 BOTTLE (71335-2489-9)Sep 18, 2024

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