Divalproex Sodium (Page 15 of 15)

Principal Display Panel

NDC: 51655-365-52

Label
(click image for full-size original)
DIVALPROEX SODIUM divalproex sodium tablet, delayed release
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:51655-365(NDC:29300-139)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DIVALPROEX SODIUM (VALPROIC ACID) VALPROIC ACID 250 mg
Inactive Ingredients
Ingredient Name Strength
ALCOHOL
BUTYL ALCOHOL
D&C RED NO. 30
FD&C BLUE NO. 2
FERRIC OXIDE RED
FERROSOFERRIC OXIDE
HYPROMELLOSE 2910 (6 MPA.S)
ISOPROPYL ALCOHOL
LACTOSE MONOHYDRATE
METHACRYLIC ACID AND ETHYL ACRYLATE COPOLYMER
MICROCRYSTALLINE CELLULOSE 112
POLYETHYLENE GLYCOL 3000
POVIDONE, UNSPECIFIED
PROPYLENE GLYCOL
SHELLAC
SILICON DIOXIDE
SODIUM BICARBONATE
SODIUM LAURYL SULFATE
STARCH, CORN
TALC
TITANIUM DIOXIDE
TRIACETIN
TRIETHYL CITRATE
VANILLIN
Product Characteristics
Color pink Score no score
Shape OVAL Size 14mm
Flavor Imprint Code UL;250
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:51655-365-52 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA079163 05/29/2020
Labeler — Northwind Pharmaceuticals (036986393)
Registrant — Northwind Pharmaceuticals (036986393)
Establishment
Name Address ID/FEI Operations
Northwind Pharmaceuticals 036986393 repack (51655-365)

Revised: 01/2022 Northwind Pharmaceuticals

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