NDC 71335-9612 – Cetirizine Hydrochloride

Cetirizine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral

Human Otc Drug

Product NDC71335-9612

Product details

Brand name
Cetirizine Hydrochloride
Generic name
Cetirizine Hydrochloride Tablets
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078343
Marketed since
December 17, 2018
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
71335-9612-130 TABLET, FILM COATED in 1 BOTTLE (71335-9612-1)Jan 3, 2023
71335-9612-214 TABLET, FILM COATED in 1 BOTTLE (71335-9612-2)Jan 3, 2023
71335-9612-37 TABLET, FILM COATED in 1 BOTTLE (71335-9612-3)Jan 3, 2023
71335-9612-410 TABLET, FILM COATED in 1 BOTTLE (71335-9612-4)Jan 3, 2023
71335-9612-515 TABLET, FILM COATED in 1 BOTTLE (71335-9612-5)Jan 3, 2023
71335-9612-690 TABLET, FILM COATED in 1 BOTTLE (71335-9612-6)Jan 3, 2023
71335-9612-720 TABLET, FILM COATED in 1 BOTTLE (71335-9612-7)Jan 3, 2023
71335-9612-860 TABLET, FILM COATED in 1 BOTTLE (71335-9612-8)Jan 3, 2023
71335-9612-9100 TABLET, FILM COATED in 1 BOTTLE (71335-9612-9)Jan 3, 2023

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