NDC 82804-232 – Levocetirizine Dihydrochloride

Levocetirizine Dihydrochloride 5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC82804-232

Product details

Brand name
Levocetirizine Dihydrochloride
Generic name
Levocetirizine Dihydrochloride
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090199
Marketed since
September 6, 2011
Listing expires
December 31, 2026
Pharmacologic class
Histamine-1 Receptor Antagonist

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
82804-232-3030 TABLET, FILM COATED in 1 BOTTLE (82804-232-30)Jul 30, 2025

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