NDC 16571-401 – Cetirizine Hydrochloride

Cetirizine Hydrochloride 5 mg/1 · Tablet · Oral

Human Otc Drug 1 recall

Product NDC16571-401

Product details

Brand name
Cetirizine Hydrochloride
Generic name
Cetirizine Hydrochloride
Labeler
Rising Pharma Holdings, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077829
Marketed since
October 1, 2009
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 (1)

Package NDCDescriptionSince
16571-401-10100 TABLET in 1 BOTTLE (16571-401-10)Oct 1, 2009

Recalls mentioning this NDC

Other Cetirizine hydrochloride products