Chenopodium Anthelminticum

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
6354548101
200 PELLET in 1 VIAL, GLASS (63545-481-01)
ndc11
6354548102
500 PELLET in 1 VIAL, GLASS (63545-481-02)
ndc11
6354548103
3000 PELLET in 1 BOTTLE, GLASS (63545-481-03)
ndc11
6354548104
10000 PELLET in 1 BOTTLE, GLASS (63545-481-04)

Annotations

UNII (FDA Substance ID)

4H5RSU087I

DYSPHANIA AMBROSIOIDES WHOLE

RxCUI 1342490

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "4H5RSU087I",
    "rxcui": "1342490",
    "inchikey": null,
    "display_name": "DYSPHANIA AMBROSIOIDES WHOLE",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "6c447c8c-5a59-0f60-e053-2a91aa0aa014": {
      "match": "brand_token",
      "title": "CHENOPODIUM ANTHELMINTICUM (DYSPHANIA AMBROSIOIDES) PELLET [BOIRON]",
      "spl_version": "3",
      "published_date": "2023-11-10"
    }
  },
  "productid": "63545-481_dec35ba0-f612-0fa9-e053-2a95a90a0898",
  "productndc": "63545-481",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "DYSPHANIA AMBROSIOIDES WHOLE",
  "proprietary_name": "Chenopodium Anthelminticum",
  "active_ingred_unit": "[hp_M]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Chenopodium Anthelminticum",
  "start_marketing_date": "20220511",
  "active_numerator_strength": "1"
}

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