Oleander

UNIISPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerHahnemann Laboratories, INC.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 4

ndc11
3766219881
200 PELLET in 1 VIAL, GLASS (37662-1988-1)
ndc11
3766219882
500 PELLET in 1 VIAL, GLASS (37662-1988-2)
ndc11
3766219883
3000 PELLET in 1 BOTTLE, GLASS (37662-1988-3)
ndc11
3766219884
10000 PELLET in 1 BOTTLE, GLASS (37662-1988-4)

Annotations

UNII (FDA Substance ID)

7KV510R6H6

NERIUM OLEANDER LEAF

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "7KV510R6H6",
    "rxcui": null,
    "inchikey": null,
    "display_name": "NERIUM OLEANDER LEAF",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "3b8cc291-49e6-2ed3-e063-6394a90ab86d": {
      "match": "brand_token",
      "title": "OLEANDER (NERIUM OLEANDER LEAF\t) PELLET [BOIRON]",
      "spl_version": "1",
      "published_date": "2025-08-18"
    }
  },
  "productid": "37662-1988_ee07f754-2b85-b456-e053-2995a90af841",
  "productndc": "37662-1988",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "NERIUM OLEANDER LEAF",
  "proprietary_name": "Oleander",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Oleander",
  "start_marketing_date": "20221121",
  "active_numerator_strength": "100"
}

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