NDC 71335-0300 – Cetirizine Hydrochloride

Cetirizine Hydrochloride 10 mg/1 · Tablet · Oral

Human Otc Drug

Product NDC71335-0300

Product details

Brand name
Cetirizine Hydrochloride
Generic name
Cetirizine Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077829
Marketed since
October 1, 2009
Listing expires
December 31, 2026
Pharmacologic class
Histamine-1 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Cetirizine hydrochloride →

Package NDC codes (9)

Package NDCDescriptionSince
71335-0300-130 TABLET in 1 BOTTLE (71335-0300-1)Feb 16, 2018
71335-0300-214 TABLET in 1 BOTTLE (71335-0300-2)Feb 20, 2018
71335-0300-37 TABLET in 1 BOTTLE (71335-0300-3)Feb 9, 2022
71335-0300-410 TABLET in 1 BOTTLE (71335-0300-4)Mar 19, 2019
71335-0300-515 TABLET in 1 BOTTLE (71335-0300-5)Feb 9, 2022
71335-0300-690 TABLET in 1 BOTTLE (71335-0300-6)Feb 16, 2018
71335-0300-720 TABLET in 1 BOTTLE (71335-0300-7)Mar 7, 2019
71335-0300-860 TABLET in 1 BOTTLE (71335-0300-8)Oct 13, 2021
71335-0300-9100 TABLET in 1 BOTTLE (71335-0300-9)May 3, 2019

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