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United States Β· US Β· US:0220-4136_f67d6f73-88d5-2031-e053-2995a90a3b09

Podophyllum peltatum

UNIISPL

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

Identification

ManufacturerBoiron
CountryUS (United States)
ATC codeβ€”
Dispensingβ€”
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs Β· 1

  • ndc11
    0220413641
    30 [hp_C] in 1 TUBE (0220-4136-41)

Annotations

UNII (FDA Substance ID)
2S713A4VP3
PODOPHYLLUM
RxCUI 324036
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "2S713A4VP3",
    "rxcui": "324036",
    "inchikey": null,
    "display_name": "PODOPHYLLUM",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "dfdc1756-e5d1-4b05-e053-2995a90ab2bd": {
      "match": "brand_token",
      "title": "PODOPHYLLUM PELT KIT REFILL (PODOPHYLLUM) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS]",
      "spl_version": "4",
      "published_date": "2025-01-30"
    }
  },
  "productid": "0220-4136_f67d6f73-88d5-2031-e053-2995a90a3b09",
  "productndc": "0220-4136",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "PODOPHYLLUM",
  "proprietary_name": "Podophyllum peltatum",
  "active_ingred_unit": "[hp_C]/30[hp_C]",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "PODOPHYLLUM",
  "start_marketing_date": "19830303",
  "active_numerator_strength": "30"
}

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Podophyllum peltatum (US) β€” Drug Database