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United States · US · US:0268-1417_028ad0ff-1a2d-4610-bf84-a0eaacaf599e

MIXED RAGWEED

UNIISPL

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

Identification

ManufacturerALK-Abello, Inc.
CountryUS (United States)
ATC code
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 2

  • ndc11
    0268141710
    10 mL in 1 VIAL (0268-1417-10)
  • ndc11
    0268141750
    50 mL in 1 VIAL (0268-1417-50)

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": "PERCUTANEOUS; SUBCUTANEOUS",
  "spl_meta": {
    "304ff4db-201a-60a4-e054-00144ff8d46c": {
      "match": "brand_token",
      "title": "MIXED BERRY SORE THROAT AND COUGH LOZENGE (DEXTROMETHORPHAN HYDROBROMIDE) LOZENGE [MEIJER DISTRIBUTION, INC.]",
      "spl_version": "8",
      "published_date": "2026-02-03"
    }
  },
  "productid": "0268-1417_028ad0ff-1a2d-4610-bf84-a0eaacaf599e",
  "productndc": "0268-1417",
  "dosage_form": "INJECTION, SOLUTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "AMBROSIA ARTEMISIIFOLIA POLLEN; AMBROSIA TRIFIDA POLLEN",
  "proprietary_name": "MIXED RAGWEED",
  "active_ingred_unit": "g/mL; g/mL",
  "application_number": "BLA103753",
  "marketing_category": "BLA",
  "nonproprietary_name": "MIXED RAGWEED",
  "start_marketing_date": "20150503",
  "active_numerator_strength": ".1; .1"
}

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