NDC 63629-4914 – Cetirizine Hydrochloride

Cetirizine Hydrochloride 5 mg/1 · Tablet · Oral

Human Otc Drug

Product NDC63629-4914

Product details

Brand name
Cetirizine Hydrochloride
Generic name
Cetirizine Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077829
Marketed since
October 1, 2009
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 (1)

Package NDCDescriptionSince
63629-4914-130 TABLET in 1 BOTTLE (63629-4914-1)Feb 19, 2013

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