NDC 51655-801 – Cetirizine Hydrochloride

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

Human Otc Drug

Product NDC51655-801

Product details

Brand name
Cetirizine Hydrochloride
Generic name
Cetirizine Hydrochloride Tablets
Labeler
Northwind Health Company, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078343
Marketed since
January 25, 2023
Listing expires
December 31, 2027
Pharmacologic class
Histamine-1 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Cetirizine hydrochloride →

Package NDC codes (3)

Package NDCDescriptionSince
51655-801-5230 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-801-52)Jan 25, 2023
51655-801-60100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-801-60)Jan 25, 2023
51655-801-8414 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-801-84)Jan 25, 2023

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