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United States · US · US:37662-0725_e3281609-460b-4982-e053-2995a90a01c5

Divalproex Sodium

In shortageUNIISPLATC N03AG01

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

Identification

ManufacturerHahnemann Laboratories, INC.
CountryUS (United States)
ATC codeN03AG01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 3

  • ndc11
    3766207251
    200 PELLET in 1 VIAL, GLASS (37662-0725-1)
  • ndc11
    3766207252
    1200 PELLET in 1 BOTTLE, GLASS (37662-0725-2)
  • ndc11
    3766207253
    4000 PELLET in 1 BOTTLE, GLASS (37662-0725-3)

Annotations

UNII (FDA Substance ID)
5VOM6GYJ0D
VALPROATE SODIUM
RxCUI 9919
DailyMed SPL labels
1 version tracked
FDA shortage
Currently in shortage
Valproate Sodium Injection
Raw payload (JSON)
{
  "unii": {
    "unii": "5VOM6GYJ0D",
    "rxcui": "9919",
    "inchikey": "AEQFSUDEHCCHBT-UHFFFAOYSA-M",
    "display_name": "VALPROATE 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": "37662-0725_e3281609-460b-4982-e053-2995a90a01c5",
  "productndc": "37662-0725",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "VALPROATE SODIUM",
  "shortage_reason": "Valproate Sodium Injection",
  "shortage_status": "current",
  "proprietary_name": "Divalproex Sodium",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Divalproex Sodium",
  "start_marketing_date": "20220706",
  "active_numerator_strength": "6"
}

Related drugs

Other records sharing ATC code N03AG01.

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