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United States · US · US:55154-4759_d6b874c5-c383-4b28-8be1-2098e4d4fd0a
Divalproex Sodium
Orange BookUNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerCardinal Health 107, LLC
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11551544759010 BLISTER PACK in 1 BAG (55154-4759-0) / 1 CAPSULE, COATED PELLETS in 1 BLISTER PACK
Annotations
UNII (FDA Substance ID)
644VL95AO6
DIVALPROEX SODIUM
RxCUI 266856
Orange Book
A078919
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": "55154-4759_d6b874c5-c383-4b28-8be1-2098e4d4fd0a",
"productndc": "55154-4759",
"dosage_form": "CAPSULE, COATED PELLETS",
"orange_book": {
"appl_no": "078919",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 125MG VALPROIC ACID",
"product_no": "001",
"approval_date": "Jan 27, 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": "ANDA078919",
"marketing_category": "ANDA",
"nonproprietary_name": "Divalproex Sodium",
"start_marketing_date": "20090318",
"active_numerator_strength": "125"
}Access this data programmatically
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