NDC 80513-731 – Cetirizine hydrochloride

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

Human Otc Drug

Product NDC80513-731

Product details

Brand name
Cetirizine hydrochloride
Generic name
Cetirizine hydrochloride
Labeler
Advanced Rx LLC
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA209274
Marketed since
May 1, 2025
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 (2)

Package NDCDescriptionSince
80513-731-05500 TABLET, COATED in 1 BOTTLE (80513-731-05)May 1, 2025
80513-731-12120 TABLET, COATED in 1 BOTTLE (80513-731-12)May 1, 2025

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