divalproex sodium d/r

Generic: divalproex sodium d/r

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name divalproex sodium d/r
Generic Name divalproex sodium d/r
Labeler direct_rx
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

divalproex sodium 250 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-636
Product ID 72189-636_3aff8f08-d8e9-cd13-e063-6394a90aa00c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078597
Listing Expiration 2026-12-31
Marketing Start 2025-07-28

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 72189636
Hyphenated Format 72189-636

Supplemental Identifiers

RxCUI
1099678
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 d/r (source: ndc)
Generic Name divalproex sodium d/r (source: ndc)
Application Number ANDA078597 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 60 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-636-60)
source: ndc

Packages (1)

72189-636-60 60 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-636-60)

Ingredients (1)

divalproex sodium (250 mg/1)

Linked Drug Pages (1)

Divalproex Sodium D/R ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3aff8f08-d8e9-cd13-e063-6394a90aa00c", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099678"], "spl_set_id": ["3aff8f08-d8e8-cd13-e063-6394a90aa00c"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-636-60)", "package_ndc": "72189-636-60", "marketing_start_date": "20250728"}], "brand_name": "Divalproex Sodium D/R", "product_id": "72189-636_3aff8f08-d8e9-cd13-e063-6394a90aa00c", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "72189-636", "generic_name": "Divalproex Sodium D/R", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex Sodium D/R", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "250 mg/1"}], "application_number": "ANDA078597", "marketing_category": "ANDA", "marketing_start_date": "20250728", "listing_expiration_date": "20261231"}