NDC 68788-4072 – Cetirizine hydrochloride

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

Human Otc Drug

Product NDC68788-4072

Product details

Brand name
Cetirizine hydrochloride
Generic name
Cetirizine Hydrochloride
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078336
Marketed since
January 27, 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 (3)

Package NDCDescriptionSince
68788-4072-31 BOTTLE in 1 CARTON (68788-4072-3) / 30 TABLET, FILM COATED in 1 BOTTLEJan 27, 2026
68788-4072-660 TABLET, FILM COATED in 1 BOTTLE (68788-4072-6)Jan 27, 2026
68788-4072-990 TABLET, FILM COATED in 1 BOTTLE (68788-4072-9)Jan 27, 2026

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