NDC 83939-0004 – Cetirizine Hydrochloride

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

Human Otc Drug

Product NDC83939-0004

Product details

Brand name
Cetirizine Hydrochloride
Generic name
Cetirizine Hydrochloride Tablets
Labeler
VERITYRX, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078343
Marketed since
December 17, 2018
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 (3)

Package NDCDescriptionSince
83939-0004-11 TABLET, FILM COATED in 1 POUCH (83939-0004-1)Nov 10, 2025
83939-0004-250 POUCH in 1 BOX, UNIT-DOSE (83939-0004-2) / 1 TABLET, FILM COATED in 1 POUCHNov 3, 2025
83939-0004-3100 POUCH in 1 BOX, UNIT-DOSE (83939-0004-3) / 1 TABLET, FILM COATED in 1 POUCHNov 3, 2025

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