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United States · US · US:70518-1781_525428a3-f546-ab78-e063-6294a90ad51c
Divalproex sodium
Orange BookUNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerREMEDYREPACK INC.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc117051817811100 POUCH in 1 BOX (70518-1781-1) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 POUCH (70518-1781-2)
Annotations
UNII (FDA Substance ID)
644VL95AO6
DIVALPROEX SODIUM
RxCUI 266856
Orange Book
A202419
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": "70518-1781_525428a3-f546-ab78-e063-6294a90ad51c",
"productndc": "70518-1781",
"dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE",
"orange_book": {
"appl_no": "202419",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 250MG VALPROIC ACID",
"product_no": "001",
"approval_date": "Jun 2, 2014"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 500MG VALPROIC ACID",
"product_no": "002",
"approval_date": "Jun 2, 2014"
}
],
"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": "ANDA202419",
"marketing_category": "ANDA",
"nonproprietary_name": "Divalproex sodium",
"start_marketing_date": "20190107",
"active_numerator_strength": "250"
}Access this data programmatically
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