NDC 48433-017 – Cetirizine Hydrochloride

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

Human Otc Drug

Product NDC48433-017

Product details

Brand name
Cetirizine Hydrochloride
Generic name
Cetirizine hydrochloride
Labeler
Safecor Health, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076677
Marketed since
April 17, 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 (1)

Package NDCDescriptionSince
48433-017-20100 BLISTER PACK in 1 CARTON (48433-017-20) / 1 TABLET, FILM COATED in 1 BLISTER PACK (48433-017-01)Apr 17, 2026

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