BETULA LENTA POLLEN

UNIISPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

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
0268106910
10 mL in 1 VIAL, MULTI-DOSE (0268-1069-10)
ndc11
0268106950
50 mL in 1 VIAL, MULTI-DOSE (0268-1069-50)

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": "SUBCUTANEOUS",
  "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": "0268-1069_a3200b5f-95f3-43cf-a26f-27a503470956",
  "productndc": "0268-1069",
  "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": "Birch White",
  "start_marketing_date": "19650101",
  "active_numerator_strength": ".1"
}

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