Arundo Mauritanica

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
6354525001
80 PELLET in 1 VIAL, GLASS (63545-250-01)
ndc11
6354525002
200 PELLET in 1 VIAL, GLASS (63545-250-02)
ndc11
6354525003
1200 PELLET in 1 BOTTLE, GLASS (63545-250-03)
ndc11
6354525004
4000 PELLET in 1 BOTTLE, GLASS (63545-250-04)

Annotations

UNII (FDA Substance ID)

ZXE7LB03WC

ARUNDO PLINIANA ROOT

RxCUI 1309800

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "ZXE7LB03WC",
    "rxcui": "1309800",
    "inchikey": null,
    "display_name": "ARUNDO PLINIANA ROOT",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "1923b4f7-a812-93d4-e063-6394a90a591b": {
      "match": "brand_token",
      "title": "ARUNDO MAURITANICA (ARUNDO PLINIANA ROOT) PELLET [BOIRON]",
      "spl_version": "1",
      "published_date": "2024-06-03"
    }
  },
  "productid": "63545-250_bed9a389-db59-1301-e053-2995a90a3577",
  "productndc": "63545-250",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ARUNDO PLINIANA ROOT",
  "proprietary_name": "Arundo Mauritanica",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Arundo Mauritanica",
  "start_marketing_date": "20210331",
  "active_numerator_strength": "30"
}

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