Melilotus Officinalis

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
3766211441
200 PELLET in 1 VIAL, GLASS (37662-1144-1)
ndc11
3766211442
500 PELLET in 1 VIAL, GLASS (37662-1144-2)
ndc11
3766211443
3000 PELLET in 1 BOTTLE, GLASS (37662-1144-3)
ndc11
3766211444
10000 PELLET in 1 BOTTLE, GLASS (37662-1144-4)

Annotations

UNII (FDA Substance ID)

GM6P02J2DX

MELILOTUS OFFICINALIS TOP

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "GM6P02J2DX",
    "rxcui": null,
    "inchikey": null,
    "display_name": "MELILOTUS OFFICINALIS TOP",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "7d792fea-6c10-0994-e053-2a91aa0a20c1": {
      "match": "brand_token",
      "title": "MELILOTUS OFFICINALIS (MELILOTUS OFFICINALIS TOP) PELLET [BOIRON]",
      "spl_version": "3",
      "published_date": "2023-11-15"
    }
  },
  "productid": "37662-1144_e537e1fc-3b8a-8ce1-e053-2a95a90a8005",
  "productndc": "37662-1144",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MELILOTUS OFFICINALIS TOP",
  "proprietary_name": "Melilotus Officinalis",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Melilotus Officinalis",
  "start_marketing_date": "20220801",
  "active_numerator_strength": "500"
}

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