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United States · US · US:22840-9320_36ac4a35-6d7b-a249-e063-6294a90a0b70

National Weed Mix

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 · 3

  • ndc11
    2284093202
    10 mL in 1 VIAL, MULTI-DOSE (22840-9320-2)
  • ndc11
    2284093204
    50 mL in 1 VIAL, MULTI-DOSE (22840-9320-4)
  • ndc11
    2284093205
    5 mL in 1 BOTTLE, DROPPER (22840-9320-5)

Annotations

UNII (FDA Substance ID)
73B14PX5FW
AMARANTHUS RETROFLEXUS POLLEN
RxCUI 851930
Raw payload (JSON)
{
  "unii": {
    "unii": "73B14PX5FW",
    "rxcui": "851930",
    "inchikey": null,
    "display_name": "AMARANTHUS RETROFLEXUS POLLEN",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS",
  "productid": "22840-9320_36ac4a35-6d7b-a249-e063-6294a90a0b70",
  "productndc": "22840-9320",
  "dosage_form": "SOLUTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "AMARANTHUS RETROFLEXUS POLLEN; AMBROSIA ARTEMISIIFOLIA POLLEN; AMBROSIA TRIFIDA POLLEN; CHENOPODIUM ALBUM POLLEN; XANTHIUM STRUMARIUM POLLEN",
  "proprietary_name": "National Weed Mix",
  "active_ingred_unit": "g/mL; g/mL; g/mL; g/mL; g/mL",
  "application_number": "BLA101833",
  "marketing_category": "BLA",
  "nonproprietary_name": "Xanthium strumarium, Ambrosia trifida, Chenopodium album, Amaranthus retroflexus and Ambrosia artemisiifolia",
  "start_marketing_date": "19810915",
  "active_numerator_strength": ".01; .01; .01; .01; .01"
}

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