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United States · US · US:27241-115_9d3c5241-441a-491e-9f94-fbca0abcad37
Divalproex sodium
Orange BookUNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAjanta Pharma USA Inc.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc112724111501100 CAPSULE, COATED PELLETS in 1 BOTTLE (27241-115-01)
- ndc112724111505500 CAPSULE, COATED PELLETS in 1 BOTTLE (27241-115-05)
- ndc1127241115101000 CAPSULE, COATED PELLETS in 1 BOTTLE (27241-115-10)
Annotations
UNII (FDA Substance ID)
644VL95AO6
DIVALPROEX SODIUM
RxCUI 266856
Orange Book
A213181
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": "27241-115_9d3c5241-441a-491e-9f94-fbca0abcad37",
"productndc": "27241-115",
"dosage_form": "CAPSULE, COATED PELLETS",
"orange_book": {
"appl_no": "213181",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 125MG VALPROIC ACID",
"product_no": "001",
"approval_date": "Mar 2, 2020"
}
],
"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": "ANDA213181",
"marketing_category": "ANDA",
"nonproprietary_name": "Divalproex sodium",
"start_marketing_date": "20200515",
"active_numerator_strength": "125"
}Access this data programmatically
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