Divalproex Sodium Extended-Release: Package Insert and Label Information (Page 8 of 8)

PACKAGE LABEL

Label Image for 53808-1061 500mg

Label Image for 500mgLabel Image for 500mg
DIVALPROEX SODIUM EXTENDED-RELEASE divalproex sodium tablet, extended release
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:53808-1061(NDC:68382-315)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DIVALPROEX SODIUM (VALPROIC ACID) VALPROIC ACID 500 mg
Product Characteristics
Color GRAY Score no score
Shape OVAL (ovaloid) Size 19mm
Flavor Imprint Code a;HC
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:53808-1061-1 30 TABLET, EXTENDED RELEASE (TABLET) in 1 BLISTER PACK None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA AUTHORIZED GENERIC NDA021168 11/01/2014
Labeler — State of Florida DOH Central Pharmacy (829348114)
Establishment
Name Address ID/FEI Operations
State of Florida DOH Central Pharmacy 829348114 repack (53808-1061)

Revised: 01/2015 State of Florida DOH Central Pharmacy

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