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United States · US · US:22840-5701_36abfd47-fc5e-43c4-e063-6394a90a8731
Apricot
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
- ndc11228405701210 mL in 1 VIAL, MULTI-DOSE (22840-5701-2)
- ndc1122840570155 mL in 1 BOTTLE, DROPPER (22840-5701-5)
Annotations
UNII (FDA Substance ID)
269CJD5GZ9
APRICOT
RxCUI 1353891
Raw payload (JSON)
{
"unii": {
"unii": "269CJD5GZ9",
"rxcui": "1353891",
"inchikey": null,
"display_name": "APRICOT",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS",
"productid": "22840-5701_36abfd47-fc5e-43c4-e063-6394a90a8731",
"productndc": "22840-5701",
"dosage_form": "SOLUTION",
"dea_schedule": null,
"product_type": "NON-STANDARDIZED ALLERGENIC",
"substance_name": "APRICOT",
"proprietary_name": "Apricot",
"active_ingred_unit": "g/mL",
"application_number": "BLA101833",
"marketing_category": "BLA",
"nonproprietary_name": "Prunus armeniaca",
"start_marketing_date": "19810915",
"active_numerator_strength": ".025"
}Access this data programmatically
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