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United States · US · US:49643-314_36ad1e17-751d-e226-e063-6394a90ab328
Redroot Pigweed Pollen
UNII
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAllermed Laboratories, Inc.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc1149643314055 mL in 1 VIAL, MULTI-DOSE (49643-314-05)
- ndc11496433141010 mL in 1 VIAL, MULTI-DOSE (49643-314-10)
- ndc11496433143030 mL in 1 VIAL, MULTI-DOSE (49643-314-30)
- ndc11496433145050 mL in 1 VIAL, MULTI-DOSE (49643-314-50)
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": "CUTANEOUS; INTRADERMAL; SUBCUTANEOUS",
"productid": "49643-314_36ad1e17-751d-e226-e063-6394a90ab328",
"productndc": "49643-314",
"dosage_form": "INJECTION",
"dea_schedule": null,
"product_type": "NON-STANDARDIZED ALLERGENIC",
"substance_name": "AMARANTHUS RETROFLEXUS POLLEN",
"proprietary_name": "Redroot Pigweed Pollen",
"active_ingred_unit": "g/mL",
"application_number": "BLA102211",
"marketing_category": "BLA",
"nonproprietary_name": "Amaranthus retroflexus",
"start_marketing_date": "19740312",
"active_numerator_strength": ".05"
}Access this data programmatically
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