Standardized Redtop Pollen

UNIISPL

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
2284002072
10 mL in 1 VIAL, MULTI-DOSE (22840-0207-2)
ndc11
2284002074
50 mL in 1 VIAL, MULTI-DOSE (22840-0207-4)
ndc11
2284002075
5 mL in 1 BOTTLE, DROPPER (22840-0207-5)

Annotations

UNII (FDA Substance ID)

HU8V6E7HOA

AGROSTIS GIGANTEA POLLEN

RxCUI 851870

DailyMed SPL labels

1 version tracked

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",
  "spl_meta": {
    "3e65b958-03cd-4f8c-a6a0-990b53ae7ab4": {
      "match": "brand_token",
      "title": "STANDARDIZED CAT PELT INJECTION, SOLUTION [JUBILANT HOLLISTERSTIER LLC]",
      "spl_version": "17",
      "published_date": "2026-04-06"
    }
  },
  "productid": "22840-0207_37385fc6-1cdd-8aa6-e063-6294a90a6017",
  "productndc": "22840-0207",
  "dosage_form": "SOLUTION",
  "dea_schedule": null,
  "product_type": "STANDARDIZED ALLERGENIC",
  "substance_name": "AGROSTIS GIGANTEA POLLEN",
  "proprietary_name": "Standardized Redtop Pollen",
  "active_ingred_unit": "[BAU]/mL",
  "application_number": "BLA101840",
  "marketing_category": "BLA",
  "nonproprietary_name": "Agrostis alba",
  "start_marketing_date": "19680915",
  "active_numerator_strength": "10000"
}

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