MIDWEST MIX OF STANDARDIZED GRASS

UNII

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

Identification

ManufacturerALK-Abello, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
0268807750
53 mL in 1 VIAL (0268-8077-50)

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": "SUBCUTANEOUS",
  "productid": "0268-8077_f4170117-0559-46bb-a4fb-66138c6a9874",
  "productndc": "0268-8077",
  "dosage_form": "INJECTION, SOLUTION",
  "dea_schedule": null,
  "product_type": "STANDARDIZED ALLERGENIC",
  "substance_name": "AGROSTIS GIGANTEA POLLEN; DACTYLIS GLOMERATA POLLEN; PHLEUM PRATENSE POLLEN; POA PRATENSIS POLLEN",
  "proprietary_name": "MIDWEST MIX OF STANDARDIZED GRASS",
  "active_ingred_unit": "[BAU]/mL; [BAU]/mL; [BAU]/mL; [BAU]/mL",
  "application_number": "BLA103058",
  "marketing_category": "BLA",
  "nonproprietary_name": "AGROSTIS GIGANTEA POLLEN, DACTYLIS GLOMERATA POLLEN, PHLEUM PRATENSE POLLEN and POA PRATENSIS POLLEN",
  "start_marketing_date": "19971218",
  "active_numerator_strength": "20000; 20000; 40000; 20000"
}

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