NDC 71205-210 – Levocetirizine Dihydrochloride

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

Human Prescription Drug

Product NDC71205-210

Product details

Brand name
Levocetirizine Dihydrochloride
Generic name
levocetirizine Dihydrochloride
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202046
Marketed since
September 30, 2013
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 (3)

Package NDCDescriptionSince
71205-210-3030 TABLET, FILM COATED in 1 BOTTLE (71205-210-30)Jan 1, 2019
71205-210-6060 TABLET, FILM COATED in 1 BOTTLE (71205-210-60)Jan 1, 2019
71205-210-9090 TABLET, FILM COATED in 1 BOTTLE (71205-210-90)Jan 1, 2019

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