NDC 68788-8435 – Cetirizine Hydrochloride

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

Human Otc Drug

Product NDC68788-8435

Product details

Brand name
Cetirizine Hydrochloride
Generic name
Cetirizine Hydrochloride Tablets
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078343
Marketed since
April 27, 2023
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
68788-8435-330 TABLET, FILM COATED in 1 BOTTLE (68788-8435-3)Apr 27, 2023
68788-8435-660 TABLET, FILM COATED in 1 BOTTLE (68788-8435-6)Apr 27, 2023
68788-8435-990 TABLET, FILM COATED in 1 BOTTLE (68788-8435-9)Apr 27, 2023

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