NDC 51655-194 – Cetirizine

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

Human Otc Drug

Product NDC51655-194

Product details

Brand name
Cetirizine
Generic name
Cetirizine Hydrochloride
Labeler
Northwind Health Company, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078336
Marketed since
October 18, 2022
Listing expires
December 31, 2027
Pharmacologic class
Histamine-1 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Cetirizine →

Package NDC codes (3)

Package NDCDescriptionSince
51655-194-2690 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-194-26)Nov 15, 2022
51655-194-5230 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-194-52)Mar 2, 2023
51655-194-60100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-194-60)Oct 18, 2022

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