DIVALPROEX SODIUM- divalproex sodium pellet 
Hahnemann 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:37662-0727
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
VALPROATE SODIUM (UNII: 5VOM6GYJ0D) (VALPROIC ACID - UNII:614OI1Z5WI) VALPROIC ACID30 [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:37662-0727-180 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/06/2022
2NDC:37662-0727-2200 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/06/2022
3NDC:37662-0727-31200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/06/2022
4NDC:37662-0727-44000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/06/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic07/06/2022
DIVALPROEX SODIUM 
divalproex sodium pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-0728
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
VALPROATE SODIUM (UNII: 5VOM6GYJ0D) (VALPROIC ACID - UNII:614OI1Z5WI) VALPROIC ACID100 [hp_C]
Inactive Ingredients
Ingredient NameStrength
SUCROSE (UNII: C151H8M554)  
Product Characteristics
ColorwhiteScoreno score
ShapeROUNDSize2mm
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:37662-0728-1200 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/06/2022
2NDC:37662-0728-2500 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/06/2022
3NDC:37662-0728-33000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/06/2022
4NDC:37662-0728-410000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/06/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic07/06/2022
DIVALPROEX SODIUM 
divalproex sodium pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-0730
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
VALPROATE SODIUM (UNII: 5VOM6GYJ0D) (VALPROIC ACID - UNII:614OI1Z5WI) VALPROIC ACID500 [hp_C]
Inactive Ingredients
Ingredient NameStrength
SUCROSE (UNII: C151H8M554)  
Product Characteristics
ColorwhiteScoreno score
ShapeROUNDSize2mm
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:37662-0730-1200 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/06/2022
2NDC:37662-0730-2500 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/06/2022
3NDC:37662-0730-33000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/06/2022
4NDC:37662-0730-410000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/06/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic07/06/2022
DIVALPROEX SODIUM 
divalproex sodium pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-0726
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
VALPROATE SODIUM (UNII: 5VOM6GYJ0D) (VALPROIC ACID - UNII:614OI1Z5WI) VALPROIC ACID12 [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:37662-0726-1200 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/06/2022
2NDC:37662-0726-21200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/06/2022
3NDC:37662-0726-34000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/06/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic07/06/2022
DIVALPROEX SODIUM 
divalproex sodium pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-0729
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
VALPROATE SODIUM (UNII: 5VOM6GYJ0D) (VALPROIC ACID - UNII:614OI1Z5WI) VALPROIC ACID200 [hp_C]
Inactive Ingredients
Ingredient NameStrength
SUCROSE (UNII: C151H8M554)  
Product Characteristics
ColorwhiteScoreno score
ShapeROUNDSize2mm
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:37662-0729-1200 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/06/2022
2NDC:37662-0729-2500 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/06/2022
3NDC:37662-0729-33000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/06/2022
4NDC:37662-0729-410000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/06/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic07/06/2022
DIVALPROEX SODIUM 
divalproex sodium pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-0725
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
VALPROATE SODIUM (UNII: 5VOM6GYJ0D) (VALPROIC ACID - UNII:614OI1Z5WI) VALPROIC ACID6 [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:37662-0725-1200 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/06/2022
2NDC:37662-0725-21200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/06/2022
3NDC:37662-0725-34000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/06/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic07/06/2022
DIVALPROEX SODIUM 
divalproex sodium pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-0731
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
VALPROATE SODIUM (UNII: 5VOM6GYJ0D) (VALPROIC ACID - UNII:614OI1Z5WI) VALPROIC ACID1 [hp_M]
Inactive Ingredients
Ingredient NameStrength
SUCROSE (UNII: C151H8M554)  
Product Characteristics
ColorwhiteScoreno score
ShapeROUNDSize2mm
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:37662-0731-1200 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/06/2022
2NDC:37662-0731-2500 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/06/2022
3NDC:37662-0731-33000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/06/2022
4NDC:37662-0731-410000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/06/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic07/06/2022
DIVALPROEX SODIUM 
divalproex sodium pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-0732
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
VALPROATE SODIUM (UNII: 5VOM6GYJ0D) (VALPROIC ACID - UNII:614OI1Z5WI) VALPROIC ACID1 [hp_Q]
Inactive Ingredients
Ingredient NameStrength
SUCROSE (UNII: C151H8M554)  
Product Characteristics
ColorwhiteScoreno score
ShapeROUNDSize1mm
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:37662-0732-110000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/06/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic07/06/2022
Labeler - Hahnemann Laboratories, INC. (147098081)
Establishment
NameAddressID/FEIBusiness Operations
Hahnemann Laboratories, INC.147098081manufacture(37662-0725, 37662-0726, 37662-0727, 37662-0728, 37662-0729, 37662-0730, 37662-0731, 37662-0732)

Revised: 7/2022
Document Id: e3281609-460b-4982-e053-2995a90a01c5
Set id: e3281609-460a-4982-e053-2995a90a01c5
Version: 1
Effective Time: 20220706
 
Hahnemann Laboratories, INC.