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United States Β· US Β· US:0268-1531_a3200b5f-95f3-43cf-a26f-27a503470956

AMBROSIA ARTEMISIIFOLIA POLLEN

UNIISPL

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerALK-Abello, Inc.
CountryUS (United States)
ATC codeβ€”
Dispensingβ€”
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs Β· 2

  • ndc11
    0268153110
    10 mL in 1 VIAL, MULTI-DOSE (0268-1531-10)
  • ndc11
    0268153150
    50 mL in 1 VIAL, MULTI-DOSE (0268-1531-50)

Annotations

UNII (FDA Substance ID)
K20Y81ACO3
AMBROSIA ARTEMISIIFOLIA POLLEN
RxCUI 896135
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "K20Y81ACO3",
    "rxcui": "896135",
    "inchikey": null,
    "display_name": "AMBROSIA ARTEMISIIFOLIA POLLEN",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "SUBCUTANEOUS",
  "spl_meta": {
    "8427717f-4d1a-54b5-e053-2a91aa0a3d00": {
      "match": "brand_token",
      "title": "AMBROSIA ARTEMISIAEFOLIA (AMBROSIA ARTEMISIIFOLIA\t) PELLET [BOIRON]",
      "spl_version": "8",
      "published_date": "2024-02-09"
    }
  },
  "productid": "0268-1531_a3200b5f-95f3-43cf-a26f-27a503470956",
  "productndc": "0268-1531",
  "dosage_form": "INJECTION, SOLUTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "AMBROSIA ARTEMISIIFOLIA POLLEN",
  "proprietary_name": "AMBROSIA ARTEMISIIFOLIA POLLEN",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA103753",
  "marketing_category": "BLA",
  "nonproprietary_name": "Ragweed Short",
  "start_marketing_date": "19650101",
  "active_numerator_strength": ".1"
}

Access this data programmatically

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AMBROSIA ARTEMISIIFOLIA POLLEN (US) β€” Drug Database