NDC 71205-709 – Cetirizine Hydrochloride

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

Human Otc Drug

Product NDC71205-709

Product details

Brand name
Cetirizine Hydrochloride
Generic name
Cetirizine Hydrochloride Tablets
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078343
Marketed since
December 17, 2018
Listing expires
December 31, 2027
Pharmacologic class
Histamine-1 Receptor Antagonist

Active ingredients

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

Package NDC codes (6)

Package NDCDescriptionSince
71205-709-00100 TABLET, FILM COATED in 1 BOTTLE (71205-709-00)Jul 8, 2025
71205-709-066 TABLET, FILM COATED in 1 BOTTLE (71205-709-06)Oct 31, 2022
71205-709-1010 TABLET, FILM COATED in 1 BOTTLE (71205-709-10)Oct 31, 2022
71205-709-2020 TABLET, FILM COATED in 1 BOTTLE (71205-709-20)Mar 4, 2026
71205-709-3030 TABLET, FILM COATED in 1 BOTTLE (71205-709-30)Oct 31, 2022
71205-709-9090 TABLET, FILM COATED in 1 BOTTLE (71205-709-90)Oct 31, 2022

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