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United States Β· US Β· US:62332-821_650146da-3899-4750-8c6e-954ddd19f23a

Divalproex sodium

Orange BookUNIISPL

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerAlembic Pharmaceuticals Inc.
CountryUS (United States)
ATC codeβ€”
Dispensingβ€”
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs Β· 4

  • ndc11
    6233282110
    100 BLISTER PACK in 1 CARTON (62332-821-10) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
  • ndc11
    6233282131
    100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62332-821-31)
  • ndc11
    6233282171
    500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62332-821-71)
  • ndc11
    6233282191
    1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62332-821-91)

Annotations

UNII (FDA Substance ID)
644VL95AO6
DIVALPROEX SODIUM
RxCUI 266856
Orange Book
A218793
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": "62332-821_650146da-3899-4750-8c6e-954ddd19f23a",
  "productndc": "62332-821",
  "dosage_form": "CAPSULE, DELAYED RELEASE",
  "orange_book": {
    "appl_no": "218793",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 125MG VALPROIC ACID",
        "product_no": "001",
        "approval_date": "Dec 19, 2024"
      }
    ],
    "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": "ANDA218793",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Divalproex sodium",
  "start_marketing_date": "20241223",
  "active_numerator_strength": "125"
}

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Divalproex sodium (US) β€” Drug Database