Melilotus Alba

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
3766224971
200 PELLET in 1 VIAL, GLASS (37662-2497-1)
ndc11
3766224972
500 PELLET in 1 VIAL, GLASS (37662-2497-2)
ndc11
3766224973
3000 PELLET in 1 BOTTLE, GLASS (37662-2497-3)
ndc11
3766224974
10000 PELLET in 1 BOTTLE, GLASS (37662-2497-4)

Annotations

UNII (FDA Substance ID)

123T84GFBH

MELILOTUS ALBUS TOP

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "123T84GFBH",
    "rxcui": null,
    "inchikey": null,
    "display_name": "MELILOTUS ALBUS 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": "37662-2497_f31d91d4-3254-7100-e053-2995a90a10f2",
  "productndc": "37662-2497",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MELILOTUS ALBUS TOP",
  "proprietary_name": "Melilotus Alba",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Melilotus Alba",
  "start_marketing_date": "20230125",
  "active_numerator_strength": "200"
}

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