NDC 71610-862 – Cetirizine hydrochloride

Cetirizine Hydrochloride 10 mg/1 · Tablet · Oral

Human Otc Drug

Product NDC71610-862

Product details

Brand name
Cetirizine hydrochloride
Generic name
Cetirizine Hydrochloride
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078336
Marketed since
December 27, 2007
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 (2)

Package NDCDescriptionSince
71610-862-3030 TABLET in 1 BOTTLE (71610-862-30)Oct 28, 2024
71610-862-6090 TABLET in 1 BOTTLE (71610-862-60)Oct 28, 2024

Other Cetirizine hydrochloride products