DIVALPROEX SODIUM pellet
Divalproex Sodium by
Drug Labeling and Warnings
Divalproex Sodium by is a Homeopathic medication manufactured, distributed, or labeled by Hahnemann Laboratories, INC.. Drug facts, warnings, and ingredients follow.
Drug Details [pdf]
- ACTIVE INGREDIENT
- DOSAGE FORMS & STRENGTHS
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- PREGNANCY OR BREAST FEEDING
- ASK DOCTOR
- KEEP OUT OF REACH OF CHILDREN
- INSTRUCTIONS FOR USE
- DOSAGE & ADMINISTRATION
- ROUTE, METHOD AND FREQUENCY OF ADMINISTRATION
- INACTIVE INGREDIENT
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
DIVALPROEX SODIUM
divalproex sodium pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-0727 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength VALPROATE SODIUM (UNII: 5VOM6GYJ0D) (VALPROIC ACID - UNII:614OI1Z5WI) VALPROIC ACID 30 [hp_C] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 3mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 37662-0727-1 80 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/06/2022 2 NDC: 37662-0727-2 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/06/2022 3 NDC: 37662-0727-3 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/06/2022 4 NDC: 37662-0727-4 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/06/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/06/2022 DIVALPROEX SODIUM
divalproex sodium pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-0728 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength VALPROATE SODIUM (UNII: 5VOM6GYJ0D) (VALPROIC ACID - UNII:614OI1Z5WI) VALPROIC ACID 100 [hp_C] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 2mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 37662-0728-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/06/2022 2 NDC: 37662-0728-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/06/2022 3 NDC: 37662-0728-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/06/2022 4 NDC: 37662-0728-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/06/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/06/2022 DIVALPROEX SODIUM
divalproex sodium pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-0730 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength VALPROATE SODIUM (UNII: 5VOM6GYJ0D) (VALPROIC ACID - UNII:614OI1Z5WI) VALPROIC ACID 500 [hp_C] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 2mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 37662-0730-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/06/2022 2 NDC: 37662-0730-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/06/2022 3 NDC: 37662-0730-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/06/2022 4 NDC: 37662-0730-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/06/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/06/2022 DIVALPROEX SODIUM
divalproex sodium pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-0726 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength VALPROATE SODIUM (UNII: 5VOM6GYJ0D) (VALPROIC ACID - UNII:614OI1Z5WI) VALPROIC ACID 12 [hp_C] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 3mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 37662-0726-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/06/2022 2 NDC: 37662-0726-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/06/2022 3 NDC: 37662-0726-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/06/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/06/2022 DIVALPROEX SODIUM
divalproex sodium pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-0729 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength VALPROATE SODIUM (UNII: 5VOM6GYJ0D) (VALPROIC ACID - UNII:614OI1Z5WI) VALPROIC ACID 200 [hp_C] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 2mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 37662-0729-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/06/2022 2 NDC: 37662-0729-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/06/2022 3 NDC: 37662-0729-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/06/2022 4 NDC: 37662-0729-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/06/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/06/2022 DIVALPROEX SODIUM
divalproex sodium pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-0725 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength VALPROATE SODIUM (UNII: 5VOM6GYJ0D) (VALPROIC ACID - UNII:614OI1Z5WI) VALPROIC ACID 6 [hp_C] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 3mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 37662-0725-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/06/2022 2 NDC: 37662-0725-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/06/2022 3 NDC: 37662-0725-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/06/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/06/2022 DIVALPROEX SODIUM
divalproex sodium pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-0731 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength VALPROATE SODIUM (UNII: 5VOM6GYJ0D) (VALPROIC ACID - UNII:614OI1Z5WI) VALPROIC ACID 1 [hp_M] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 2mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 37662-0731-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/06/2022 2 NDC: 37662-0731-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/06/2022 3 NDC: 37662-0731-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/06/2022 4 NDC: 37662-0731-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/06/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/06/2022 DIVALPROEX SODIUM
divalproex sodium pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-0732 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength VALPROATE SODIUM (UNII: 5VOM6GYJ0D) (VALPROIC ACID - UNII:614OI1Z5WI) VALPROIC ACID 1 [hp_Q] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 1mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 37662-0732-1 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/06/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/06/2022 Labeler - Hahnemann Laboratories, INC. (147098081) Establishment Name Address ID/FEI Business Operations Hahnemann Laboratories, INC. 147098081 manufacture(37662-0725, 37662-0726, 37662-0727, 37662-0728, 37662-0729, 37662-0730, 37662-0731, 37662-0732)
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