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United States · US · US:0074-6114_d038b7e9-b014-4771-93be-90aeeaece03d
Depakote
Orange BookUNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAbbVie Inc.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc110074611413100 CAPSULE in 1 BOTTLE (0074-6114-13)
Annotations
UNII (FDA Substance ID)
644VL95AO6
DIVALPROEX SODIUM
RxCUI 266856
Orange Book
N019680
AB
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": "0074-6114_d038b7e9-b014-4771-93be-90aeeaece03d",
"productndc": "0074-6114",
"dosage_form": "CAPSULE",
"orange_book": {
"appl_no": "019680",
"products": [
{
"rs": true,
"rld": true,
"te_code": "AB",
"strength": "EQ 125MG VALPROIC ACID",
"product_no": "001",
"approval_date": "Sep 12, 1989"
}
],
"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": "NDA019680",
"marketing_category": "NDA",
"nonproprietary_name": "Divalproex Sodium",
"start_marketing_date": "19890912",
"active_numerator_strength": "125"
}Access this data programmatically
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