NDC 42571-122 – Levocetirizine Dihydrochloride

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

Human Prescription Drug

Product NDC42571-122

Product details

Brand name
Levocetirizine Dihydrochloride
Generic name
levocetirizine Dihydrochloride
Labeler
Micro Labs Limited
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 (4)

Package NDCDescriptionSince
42571-122-05500 TABLET, FILM COATED in 1 BOTTLE (42571-122-05)Sep 30, 2013
42571-122-3030 TABLET, FILM COATED in 1 BOTTLE (42571-122-30)Sep 30, 2013
42571-122-3210 BLISTER PACK in 1 CARTON (42571-122-32) / 10 TABLET, FILM COATED in 1 BLISTER PACK (42571-122-11)Sep 30, 2013
42571-122-9090 TABLET, FILM COATED in 1 BOTTLE (42571-122-90)Sep 30, 2013

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