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United States · US · US:22840-5709_36abfd47-fc5e-43c4-e063-6394a90a8731
Buckwheat
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 · 2
- ndc11228405709210 mL in 1 VIAL, MULTI-DOSE (22840-5709-2)
- ndc1122840570955 mL in 1 BOTTLE, DROPPER (22840-5709-5)
Annotations
UNII (FDA Substance ID)
N0Y68724R3
BUCKWHEAT
RxCUI 899394
Raw payload (JSON)
{
"unii": {
"unii": "N0Y68724R3",
"rxcui": "899394",
"inchikey": null,
"display_name": "BUCKWHEAT",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS",
"productid": "22840-5709_36abfd47-fc5e-43c4-e063-6394a90a8731",
"productndc": "22840-5709",
"dosage_form": "SOLUTION",
"dea_schedule": null,
"product_type": "NON-STANDARDIZED ALLERGENIC",
"substance_name": "BUCKWHEAT",
"proprietary_name": "Buckwheat",
"active_ingred_unit": "g/mL",
"application_number": "BLA101833",
"marketing_category": "BLA",
"nonproprietary_name": "Fagopyrum esculentum",
"start_marketing_date": "19810915",
"active_numerator_strength": ".05"
}Access this data programmatically
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