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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

  • ndc11
    2284057012
    10 mL in 1 VIAL, MULTI-DOSE (22840-5701-2)
  • ndc11
    2284057015
    5 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"
}

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