NDC 81469-353 – Cetirizine Hydrochloride

Cetirizine Hydrochloride 10 mg/1 · Tablet · Oral

Human Otc Drug

Product NDC81469-353

Product details

Brand name
Cetirizine Hydrochloride
Generic name
Cetirizine Hydrochloride
Labeler
First Nation Group, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076047
Marketed since
May 29, 2026
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 (4)

Package NDCDescriptionSince
81469-353-01100 TABLET in 1 BOTTLE (81469-353-01)Jun 1, 2026
81469-353-03300 TABLET in 1 BOTTLE (81469-353-03)Jun 1, 2026
81469-353-05500 TABLET in 1 BOTTLE (81469-353-05)Jun 1, 2026
81469-353-9090 TABLET in 1 BOTTLE (81469-353-90)Jun 1, 2026

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