divalproex sodium

Generic: divalproex sodium

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name divalproex sodium
Generic Name divalproex sodium
Labeler proficient rx lp
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

divalproex sodium 250 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 82804-233
Product ID 82804-233_15ffe3d8-d483-4c45-adc4-1cc8a5b68d19
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078853
Listing Expiration 2026-12-31
Marketing Start 2024-06-26

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 82804233
Hyphenated Format 82804-233

Supplemental Identifiers

RxCUI
1099678
UPC
0382804233304
UNII
644VL95AO6

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)
Application Number ANDA078853 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 30 TABLET, DELAYED RELEASE in 1 BOTTLE (82804-233-30)
source: ndc

Packages (1)

82804-233-30 30 TABLET, DELAYED RELEASE in 1 BOTTLE (82804-233-30)

Ingredients (1)

divalproex sodium (250 mg/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": "15ffe3d8-d483-4c45-adc4-1cc8a5b68d19", "openfda": {"upc": ["0382804233304"], "unii": ["644VL95AO6"], "rxcui": ["1099678"], "spl_set_id": ["15ffe3d8-d483-4c45-adc4-1cc8a5b68d19"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (82804-233-30)", "package_ndc": "82804-233-30", "marketing_start_date": "20250806"}], "brand_name": "divalproex sodium", "product_id": "82804-233_15ffe3d8-d483-4c45-adc4-1cc8a5b68d19", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "82804-233", "generic_name": "divalproex sodium", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "divalproex sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "250 mg/1"}], "application_number": "ANDA078853", "marketing_category": "ANDA", "marketing_start_date": "20240626", "listing_expiration_date": "20261231"}