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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
- ndc11228409320210 mL in 1 VIAL, MULTI-DOSE (22840-9320-2)
- ndc11228409320450 mL in 1 VIAL, MULTI-DOSE (22840-9320-4)
- ndc1122840932055 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"
}Access this data programmatically
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