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United States Β· US Β· US:0268-6610_22a0440f-2b25-45c4-997a-ea67c4ccea74

BETULA LENTA 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· 1

  • ndc11
    0268661006
    5 mL in 1 VIAL, MULTI-DOSE (0268-6610-06)

Annotations

UNII (FDA Substance ID)
JQ5HI5004M
BETULA LENTA POLLEN
RxCUI 852144
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "JQ5HI5004M",
    "rxcui": "852144",
    "inchikey": null,
    "display_name": "BETULA LENTA POLLEN",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "PERCUTANEOUS",
  "spl_meta": {
    "7f436fc5-0983-4ce3-9951-e68e395bcab0": {
      "match": "brand_token",
      "title": "BETULA ARGENTUM LIQUID [URIEL PHARMACY INC.]",
      "spl_version": "4",
      "published_date": "2025-06-30"
    }
  },
  "productid": "0268-6610_22a0440f-2b25-45c4-997a-ea67c4ccea74",
  "productndc": "0268-6610",
  "dosage_form": "INJECTION, SOLUTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "BETULA LENTA POLLEN",
  "proprietary_name": "BETULA LENTA POLLEN",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA103753",
  "marketing_category": "BLA",
  "nonproprietary_name": "White Birch",
  "start_marketing_date": "19650101",
  "active_numerator_strength": ".05"
}

Access this data programmatically

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BETULA LENTA POLLEN (US) β€” Drug Database