Depakote

Orange BookUNIISPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerAbbVie Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
0074732613
100 TABLET, DELAYED RELEASE in 1 BOTTLE (0074-7326-13)

Annotations

UNII (FDA Substance ID)

644VL95AO6

DIVALPROEX SODIUM

RxCUI 266856

Orange Book

N018723

ABABAB

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "644VL95AO6",
    "rxcui": "266856",
    "inchikey": "MSRILKIQRXUYCT-UHFFFAOYSA-M",
    "display_name": "DIVALPROEX SODIUM",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "08a65cf4-7749-4ceb-6895-8f4805e2b01f": {
      "match": "brand_token",
      "title": "DEPAKOTE (DIVALPROEX SODIUM) TABLET, DELAYED RELEASE [ABBVIE INC.]",
      "spl_version": "1621",
      "published_date": "2026-04-14"
    }
  },
  "productid": "0074-7326_7cc3a0b3-93f8-4825-88e1-bf6ddb0db23d",
  "productndc": "0074-7326",
  "dosage_form": "TABLET, DELAYED RELEASE",
  "orange_book": {
    "appl_no": "018723",
    "products": [
      {
        "rs": false,
        "rld": true,
        "te_code": "AB",
        "strength": "EQ 250MG VALPROIC ACID",
        "product_no": "001",
        "approval_date": "Mar 10, 1983"
      },
      {
        "rs": true,
        "rld": true,
        "te_code": "AB",
        "strength": "EQ 500MG VALPROIC ACID",
        "product_no": "002",
        "approval_date": "Mar 10, 1983"
      },
      {
        "rs": false,
        "rld": true,
        "te_code": "AB",
        "strength": "EQ 125MG VALPROIC ACID",
        "product_no": "003",
        "approval_date": "Oct 26, 1984"
      }
    ],
    "appl_type": "N"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "DIVALPROEX SODIUM",
  "proprietary_name": "Depakote",
  "active_ingred_unit": "mg/1",
  "application_number": "NDA018723",
  "marketing_category": "NDA",
  "nonproprietary_name": "Divalproex Sodium",
  "start_marketing_date": "20230630",
  "active_numerator_strength": "250"
}

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