NDC 72789-458 – Cetirizine hydrochloride

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

Human Otc Drug

Product NDC72789-458

Product details

Brand name
Cetirizine hydrochloride
Generic name
Cetirizine Hydrochloride
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076047
Marketed since
April 23, 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 (4)

Package NDCDescriptionSince
72789-458-1010 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-458-10)Oct 23, 2025
72789-458-3030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-458-30)May 29, 2025
72789-458-51365 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-458-51)Apr 23, 2025
72789-458-9090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-458-90)May 29, 2025

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