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United States · US · US:0904-6615_d19fd110-9f66-41ec-a016-f02ec3b37b73
Divalproex sodium
Orange BookUNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerMajor Pharmaceuticals
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc110904661561100 BLISTER PACK in 1 CARTON (0904-6615-61) / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
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": "0904-6615_d19fd110-9f66-41ec-a016-f02ec3b37b73",
"productndc": "0904-6615",
"dosage_form": "CAPSULE, DELAYED RELEASE",
"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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