NDC 51672-4070 – Cetirizine Hydrochloride

Cetirizine Hydrochloride 1 mg/mL · Solution · Oral

Human Prescription Drug

Product NDC51672-4070

Product details

Brand name
Cetirizine Hydrochloride
Generic name
Cetirizine Hydrochloride
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Solution
Route
Oral
Marketing category
ANDA · ANDA076601
Marketed since
May 1, 2014
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
51672-4070-81 BOTTLE in 1 CARTON (51672-4070-8) / 120 mL in 1 BOTTLEMay 1, 2014

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