Levocetirizine Dihydrochloride 42571-0122-30

Package NDC

42571-0122-30

Manufacturer: Micro Labs Limited
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: September 30, 2013
Listing Expires: December 31, 2026
Application: ANDA202046

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Active Ingredients

Ingredient	Strength
Levocetirizine Dihydrochloride	5 mg/1

Drug Class

Histamine H1 Receptor Antagonists [MoA]Histamine-1 Receptor Antagonist [EPC]

Selected Package

42571-0122-30Selected

30 TABLET, FILM COATED in 1 BOTTLE (42571-122-30)

Other packages for this product(3)

42571-0122-05

500 TABLET, FILM COATED in 1 BOTTLE (42571-122-05)

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42571-0122-32

10 BLISTER PACK in 1 CARTON (42571-122-32) / 10 TABLET, FILM COATED in 1 BLISTER PACK (42571-122-11)

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42571-0122-90

90 TABLET, FILM COATED in 1 BOTTLE (42571-122-90)

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