Levocetirizine Dihydrochloride (Page 6 of 6)

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Levocetirizine Dihydrochloride Tablets 5 mg 90s Label Text

NDC 0093-7701- 98

Levocetirizine
Dihydrochloride
Tablets USP 5 mg

Rx only

90 TABLETS

TEVA

LEVOCETIRIZINE DIHYDROCHLORIDE levocetirizine dihydrochloride tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0093-7701
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LEVOCETIRIZINE DIHYDROCHLORIDE (LEVOCETIRIZINE) LEVOCETIRIZINE DIHYDROCHLORIDE 5 mg
Inactive Ingredients
Ingredient Name Strength
SILICON DIOXIDE
HYPROMELLOSE 2910 (5 MPA.S)
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
MICROCRYSTALLINE CELLULOSE
POLYETHYLENE GLYCOL 400
TITANIUM DIOXIDE
Product Characteristics
Color WHITE (white to off-white) Score 2 pieces
Shape OVAL Size 8mm
Flavor Imprint Code 9;3;7701
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0093-7701-98 90 TABLET, FILM COATED in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA090199 09/06/2011
Labeler — Teva Pharmaceuticals USA, Inc. (001627975)

Revised: 04/2019 Teva Pharmaceuticals USA, Inc.

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