NDC 71335-2283 – Levocetirizine dihydrochloride

Levocetirizine Dihydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2283

Product details

Brand name
Levocetirizine dihydrochloride
Generic name
Levocetirizine dihydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA203646
Marketed since
September 9, 2014
Listing expires
December 31, 2027
Pharmacologic class
Histamine-1 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Levocetirizine dihydrochloride →

Package NDC codes (3)

Package NDCDescriptionSince
71335-2283-110 TABLET in 1 BOTTLE (71335-2283-1)Nov 30, 2023
71335-2283-235 TABLET in 1 BOTTLE (71335-2283-2)Nov 30, 2023
71335-2283-35 TABLET in 1 BOTTLE (71335-2283-3)Nov 30, 2023

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