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United States · US · US:0615-8237_9acc51b3-fd1c-48a4-b620-689c38545dd5
Divalproex sodium
Orange BookUNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerNCS HealthCare of KY, LLC dba Vangard Labs
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc11061582370515 CAPSULE in 1 BLISTER PACK (0615-8237-05)
- ndc11061582372828 CAPSULE in 1 BLISTER PACK (0615-8237-28)
- ndc1106158237306 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-8237-30) / 5 CAPSULE in 1 BLISTER PACK
- ndc11061582373930 CAPSULE in 1 BLISTER PACK (0615-8237-39)
Annotations
UNII (FDA Substance ID)
644VL95AO6
DIVALPROEX SODIUM
RxCUI 266856
Orange Book
A078979
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": {
"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": "0615-8237_9acc51b3-fd1c-48a4-b620-689c38545dd5",
"productndc": "0615-8237",
"dosage_form": "CAPSULE",
"orange_book": {
"appl_no": "078979",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 125MG VALPROIC ACID",
"product_no": "001",
"approval_date": "Jan 23, 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": "ANDA078979",
"marketing_category": "ANDA",
"nonproprietary_name": "Divalproex sodium",
"start_marketing_date": "20090123",
"active_numerator_strength": "125"
}Access this data programmatically
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