K-O-R-T Standardized Grass Pollen Mix

UNII

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerGreer Laboratories, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 3

ndc11
2284002192
10 mL in 1 VIAL, MULTI-DOSE (22840-0219-2)
ndc11
2284002194
50 mL in 1 VIAL, MULTI-DOSE (22840-0219-4)
ndc11
2284002195
5 mL in 1 BOTTLE, DROPPER (22840-0219-5)

Annotations

UNII (FDA Substance ID)

HU8V6E7HOA

AGROSTIS GIGANTEA POLLEN

RxCUI 851870

Raw payload (JSON)

{
  "unii": {
    "unii": "HU8V6E7HOA",
    "rxcui": "851870",
    "inchikey": null,
    "display_name": "AGROSTIS GIGANTEA POLLEN",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS",
  "productid": "22840-0219_37385fc6-1cdd-8aa6-e063-6294a90a6017",
  "productndc": "22840-0219",
  "dosage_form": "SOLUTION",
  "dea_schedule": null,
  "product_type": "STANDARDIZED ALLERGENIC",
  "substance_name": "AGROSTIS GIGANTEA POLLEN; DACTYLIS GLOMERATA POLLEN; PHLEUM PRATENSE POLLEN; POA PRATENSIS POLLEN",
  "proprietary_name": "K-O-R-T Standardized Grass Pollen Mix",
  "active_ingred_unit": "[BAU]/mL; [BAU]/mL; [BAU]/mL; [BAU]/mL",
  "application_number": "BLA101837",
  "marketing_category": "BLA",
  "nonproprietary_name": "Poa pratensis, Dactylis glomerata, Agrostis alba and Phleum pratense",
  "start_marketing_date": "19680915",
  "active_numerator_strength": "25000; 25000; 25000; 25000"
}

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