Ptelea Trifoliata

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
3766219351
200 PELLET in 1 VIAL, GLASS (37662-1935-1)
ndc11
3766219352
500 PELLET in 1 VIAL, GLASS (37662-1935-2)
ndc11
3766219353
3000 PELLET in 1 BOTTLE, GLASS (37662-1935-3)
ndc11
3766219354
10000 PELLET in 1 BOTTLE, GLASS (37662-1935-4)

Annotations

UNII (FDA Substance ID)

5KQR6FTT0D

PTELEA TRIFOLIATA BARK

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "5KQR6FTT0D",
    "rxcui": null,
    "inchikey": null,
    "display_name": "PTELEA TRIFOLIATA BARK",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "3b8d0e54-aeee-1492-e063-6294a90a3f67": {
      "match": "brand_token",
      "title": "PTELEA TRIFOLIATA (PTELEA TRIFOLIATA BARK) PELLET [BOIRON]",
      "spl_version": "1",
      "published_date": "2025-08-18"
    }
  },
  "productid": "37662-1935_ed7b9fea-fbad-85a4-e053-2995a90a8521",
  "productndc": "37662-1935",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "PTELEA TRIFOLIATA BARK",
  "proprietary_name": "Ptelea Trifoliata",
  "active_ingred_unit": "[hp_M]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Ptelea Trifoliata",
  "start_marketing_date": "20221114",
  "active_numerator_strength": "1"
}

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