NDC 68071-2571 – Cetirizine Hydrochloride

Cetirizine Hydrochloride 10 mg/1 · Tablet · Oral

Human Otc Drug

Product NDC68071-2571

Product details

Brand name
Cetirizine Hydrochloride
Generic name
Cetirizine Hydrochloride
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077498
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 (1)

Package NDCDescriptionSince
68071-2571-77 TABLET in 1 BOTTLE (68071-2571-7)Nov 15, 2021

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