divalproex sodium

Generic: divalproex sodium

Labeler: hahnemann laboratories, inc.
NDC Directory HUMAN OTC DRUG UNAPPROVED HOMEOPATHIC Inactive Finished

Drug Facts

Product Profile

Brand Name divalproex sodium
Generic Name divalproex sodium
Labeler hahnemann laboratories, inc.
Dosage Form PELLET
Routes
ORAL
Active Ingredients

valproate sodium 500 [hp_C]/1

Manufacturer
Hahnemann Laboratories, INC.

Identifiers & Regulatory

Product NDC 37662-0730
Product ID 37662-0730_e3281609-460b-4982-e053-2995a90a01c5
Product Type HUMAN OTC DRUG
Marketing Category UNAPPROVED HOMEOPATHIC
Listing Expiration 2026-12-31
Marketing Start 2022-07-06

Pharmacologic Class

Classes
anti-epileptic agent [epc] decreased central nervous system disorganized electrical activity [pe] mood stabilizer [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 376620730
Hyphenated Format 37662-0730

Supplemental Identifiers

UNII
5VOM6GYJ0D

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name divalproex sodium (source: ndc)
Generic Name divalproex sodium (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 [hp_C]/1
source: ndc
Packaging
  • 200 PELLET in 1 VIAL, GLASS (37662-0730-1)
  • 500 PELLET in 1 VIAL, GLASS (37662-0730-2)
  • 3000 PELLET in 1 BOTTLE, GLASS (37662-0730-3)
  • 10000 PELLET in 1 BOTTLE, GLASS (37662-0730-4)
source: ndc

Packages (4)

37662-0730-1 200 PELLET in 1 VIAL, GLASS (37662-0730-1) 37662-0730-2 500 PELLET in 1 VIAL, GLASS (37662-0730-2) 37662-0730-3 3000 PELLET in 1 BOTTLE, GLASS (37662-0730-3) 37662-0730-4 10000 PELLET in 1 BOTTLE, GLASS (37662-0730-4)

Ingredients (1)

valproate sodium (500 [hp_C]/1)

Linked Drug Pages (1)

Divalproex Sodium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e3281609-460b-4982-e053-2995a90a01c5", "openfda": {"unii": ["5VOM6GYJ0D"], "spl_set_id": ["e3281609-460a-4982-e053-2995a90a01c5"], "manufacturer_name": ["Hahnemann Laboratories, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 PELLET in 1 VIAL, GLASS (37662-0730-1)", "package_ndc": "37662-0730-1", "marketing_start_date": "20220706"}, {"sample": false, "description": "500 PELLET in 1 VIAL, GLASS (37662-0730-2)", "package_ndc": "37662-0730-2", "marketing_start_date": "20220706"}, {"sample": false, "description": "3000 PELLET in 1 BOTTLE, GLASS (37662-0730-3)", "package_ndc": "37662-0730-3", "marketing_start_date": "20220706"}, {"sample": false, "description": "10000 PELLET in 1 BOTTLE, GLASS (37662-0730-4)", "package_ndc": "37662-0730-4", "marketing_start_date": "20220706"}], "brand_name": "Divalproex Sodium", "product_id": "37662-0730_e3281609-460b-4982-e053-2995a90a01c5", "dosage_form": "PELLET", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "37662-0730", "generic_name": "Divalproex Sodium", "labeler_name": "Hahnemann Laboratories, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Divalproex Sodium", "active_ingredients": [{"name": "VALPROATE SODIUM", "strength": "500 [hp_C]/1"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20220706", "listing_expiration_date": "20261231"}