BELVIQ XR Extended Release Extended Release (Page 8 of 8)

PRINCIPAL DISPLAY PANEL

NDC 62856-535-30
Belviq XR
(lorcaserin HCI)
Extended Release Tablets
20 mg
30 TabletsRx Only

PRINCIPAL DISPLAY PANEL
NDC 62856-535-30
Belviq XR
(lorcaserin HCI)
Extended Release Tablets
20 mg
30 Tablets
Rx Only
(click image for full-size original)
BELVIQ XR EXTENDED RELEASE EXTENDED RELEASE lorcaserin hydrochloride tablet, film coated, extended release
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:62856-535
Route of Administration ORAL DEA Schedule CIV
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LORCASERIN HYDROCHLORIDE ANHYDROUS (LORCASERIN) LORCASERIN HYDROCHLORIDE ANHYDROUS 20 mg
Inactive Ingredients
Ingredient Name Strength
CELLULOSE, MICROCRYSTALLINE
MANNITOL
HYPROMELLOSE 2208 (4000 MPA.S)
ETHYLCELLULOSES
HYPROMELLOSE 2910 (15 MPA.S)
SILICON DIOXIDE
POLYVINYL ALCOHOL, UNSPECIFIED
POLYETHYLENE GLYCOLS
TITANIUM DIOXIDE
TALC
FD&C YELLOW NO. 6
ALUMINUM OXIDE
FERRIC OXIDE YELLOW
FERRIC OXIDE RED
MAGNESIUM STEARATE
Product Characteristics
Color ORANGE (orange) Score no score
Shape ROUND (biconvex) Size 9mm
Flavor GRAPE (GRAPE) Imprint Code A;20
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:62856-535-30 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA208524 07/15/2016
Labeler — Eisai Inc. (831600833)

Revised: 07/2016 Eisai Inc.

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