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United States · US · US:68001-105_304dd980-5e9b-d776-e063-6394a90aa9cf
Divalproex Sodium
Orange BookUNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBluePoint Laboratories
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc116800110500100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-105-00)
- ndc116800110503500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-105-03)
Annotations
UNII (FDA Substance ID)
644VL95AO6
DIVALPROEX SODIUM
RxCUI 266856
Orange Book
A078239
ABAB
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": {
"773a289b-65ed-4045-80c5-f00e28c1c079": {
"match": "brand_token",
"title": "DIVALPROEX SODIUM CAPSULE, COATED PELLETS [AJANTA PHARMA USA INC.]",
"spl_version": "14",
"published_date": "2026-06-01"
}
},
"productid": "68001-105_304dd980-5e9b-d776-e063-6394a90aa9cf",
"productndc": "68001-105",
"dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE",
"orange_book": {
"appl_no": "078239",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 250MG VALPROIC ACID",
"product_no": "001",
"approval_date": "Feb 27, 2009"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 500MG VALPROIC ACID",
"product_no": "002",
"approval_date": "Aug 4, 2009"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "DIVALPROEX SODIUM",
"proprietary_name": "Divalproex Sodium",
"active_ingred_unit": "mg/1",
"application_number": "ANDA078239",
"marketing_category": "ANDA",
"nonproprietary_name": "Divalproex Sodium",
"start_marketing_date": "20131008",
"active_numerator_strength": "250"
}Access this data programmatically
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