Clarinex (Page 6 of 6)

Desloratadine

Label ImageLabel Image
CLARINEX desloratadine tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:50090-0765(NDC:0085-1264)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DESLORATADINE (DESLORATADINE) DESLORATADINE 5 mg
Inactive Ingredients
Ingredient Name Strength
DIBASIC CALCIUM PHOSPHATE DIHYDRATE
MICROCRYSTALLINE CELLULOSE
starch, corn
talc
carnauba wax
white wax
lactose monohydrate
HYPROMELLOSE, UNSPECIFIED
titanium dioxide
POLYETHYLENE GLYCOL, UNSPECIFIED
FD&C Blue No. 2
Aluminum Oxide
Product Characteristics
Color BLUE (LIGHT BLUE) Score no score
Shape ROUND Size 6mm
Flavor Imprint Code C5
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:50090-0765-0 30 TABLET, FILM COATED in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA021165 12/21/2001
Labeler — A-S Medication Solutions (830016429)
Establishment
Name Address ID/FEI Operations
A-S Medication Solutions 830016429 RELABEL (50090-0765), REPACK (50090-0765)

Revised: 02/2021 A-S Medication Solutions

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