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United States Β· US Β· US:0268-0156_070eea8d-3fd1-452d-89de-1dbf1c19efb2

CENTER-AL - AMBROSIA ARTEMISIIFOLIA POLLEN

UNII

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· 1

  • ndc11
    0268015630
    30 mL in 1 VIAL, MULTI-DOSE (0268-0156-30)

Annotations

UNII (FDA Substance ID)
K20Y81ACO3
AMBROSIA ARTEMISIIFOLIA POLLEN
RxCUI 896135
Raw payload (JSON)
{
  "unii": {
    "unii": "K20Y81ACO3",
    "rxcui": "896135",
    "inchikey": null,
    "display_name": "AMBROSIA ARTEMISIIFOLIA POLLEN",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "SUBCUTANEOUS",
  "productid": "0268-0156_070eea8d-3fd1-452d-89de-1dbf1c19efb2",
  "productndc": "0268-0156",
  "dosage_form": "INJECTION, SUSPENSION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "AMBROSIA ARTEMISIIFOLIA POLLEN",
  "proprietary_name": "CENTER-AL - AMBROSIA ARTEMISIIFOLIA POLLEN",
  "active_ingred_unit": "[PNU]/mL",
  "application_number": "BLA103753",
  "marketing_category": "BLA",
  "nonproprietary_name": "AMBROSIA ARTEMISIIFOLIA POLLEN",
  "start_marketing_date": "19750115",
  "active_numerator_strength": "20000"
}

Access this data programmatically

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CENTER-AL - AMBROSIA ARTEMISIIFOLIA POLLEN (US) β€” Drug Database