DIVALPROEX SODIUM- divalproex sodium pellet 
Hahnenmann Laboratories, Inc.

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

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DIVALPROEX SODIUM 
divalproex sodium pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63545-678
Route of AdministrationBUCCAL, SUBLINGUAL, ORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIVALPROEX SODIUM (UNII: 644VL95AO6) (VALPROIC ACID - UNII:614OI1Z5WI) VALPROIC ACID30 [hp_C]  in 1 [hp_C]
Inactive Ingredients
Ingredient NameStrength
SUCROSE (UNII: C151H8M554)  
Product Characteristics
ColorwhiteScoreno score
ShapeROUNDSize3mm
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63545-678-01240 [hp_C] in 1 VIAL, GLASS; Type 0: Not a Combination Product05/04/2017
Image of Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic05/04/2017
Labeler - Hahnenmann Laboratories, Inc. (147098081)
Establishment
NameAddressID/FEIBusiness Operations
Hahnemann Laboratories, Inc.147098081manufacture(63545-678)

Revised: 5/2017
Document Id: 4eb51bae-ae02-52e3-e054-00144ff8d46c
Set id: 4eb51bae-ae01-52e3-e054-00144ff8d46c
Version: 1
Effective Time: 20170504
 
Hahnenmann Laboratories, Inc.