Label: DIVALPROEX SODIUM pellet
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NDC Code(s):
37662-0725-1,
37662-0725-2,
37662-0725-3,
37662-0726-1, view more37662-0726-2, 37662-0726-3, 37662-0727-1, 37662-0727-2, 37662-0727-3, 37662-0727-4, 37662-0728-1, 37662-0728-2, 37662-0728-3, 37662-0728-4, 37662-0729-1, 37662-0729-2, 37662-0729-3, 37662-0729-4, 37662-0730-1, 37662-0730-2, 37662-0730-3, 37662-0730-4, 37662-0731-1, 37662-0731-2, 37662-0731-3, 37662-0731-4, 37662-0732-1
- Packager: Hahnemann Laboratories, INC.
- Category: HUMAN OTC DRUG LABEL
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.
Drug Label Information
Updated July 6, 2022
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- 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)
