NDC 10135-639 – Levocetirizine Dihydrochloride

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

Human Prescription Drug

Product NDC10135-639

Product details

Brand name
Levocetirizine Dihydrochloride
Generic name
levocetirizine Dihydrochloride
Labeler
Marlex Pharmaceuticals Inc
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202046
Marketed since
September 1, 2018
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 (2)

Package NDCDescriptionSince
10135-639-3030 TABLET, FILM COATED in 1 BOTTLE (10135-639-30)Sep 1, 2018
10135-639-9090 TABLET, FILM COATED in 1 BOTTLE (10135-639-90)Sep 1, 2018

Other Levocetirizine dihydrochloride products