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United States · US · US:22840-1351_36ac4a35-6d7b-a249-e063-6294a90a0b70

Prairie Mugwort Darkleaved Sagebrush

UNII

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

Identification

ManufacturerGreer Laboratories, Inc.
CountryUS (United States)
ATC code
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    2284013511
    5 mL in 1 VIAL, MULTI-DOSE (22840-1351-1)

Annotations

UNII (FDA Substance ID)
57KIJ4772H
ARTEMISIA LUDOVICIANA POLLEN
Raw payload (JSON)
{
  "unii": {
    "unii": "57KIJ4772H",
    "rxcui": null,
    "inchikey": null,
    "display_name": "ARTEMISIA LUDOVICIANA POLLEN",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS",
  "productid": "22840-1351_36ac4a35-6d7b-a249-e063-6294a90a0b70",
  "productndc": "22840-1351",
  "dosage_form": "SOLUTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "ARTEMISIA LUDOVICIANA POLLEN",
  "proprietary_name": "Prairie Mugwort Darkleaved Sagebrush",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA101833",
  "marketing_category": "BLA",
  "nonproprietary_name": "Artemisia ludoviciana",
  "start_marketing_date": "19810915",
  "active_numerator_strength": ".001"
}

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