BIRCH MIX

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
0268802410
10.5 mL in 1 VIAL (0268-8024-10)
ndc11
0268802450
53 mL in 1 VIAL (0268-8024-50)

Annotations

UNII (FDA Substance ID)

93963RFO1P

BETULA NIGRA POLLEN

RxCUI 852148

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "93963RFO1P",
    "rxcui": "852148",
    "inchikey": null,
    "display_name": "BETULA NIGRA POLLEN",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "SUBCUTANEOUS",
  "spl_meta": {
    "0fa00042-b326-6d2d-e063-6394a90a236d": {
      "match": "brand_token",
      "title": "BIRCH JUNIPER LIQUID [URIEL PHARMACY INC]",
      "spl_version": "5",
      "published_date": "2025-11-19"
    }
  },
  "productid": "0268-8024_78f45cdb-937a-4516-b8b8-3e5095a98154",
  "productndc": "0268-8024",
  "dosage_form": "INJECTION, SOLUTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "BETULA NIGRA POLLEN; BETULA POPULIFOLIA POLLEN",
  "proprietary_name": "BIRCH MIX",
  "active_ingred_unit": "g/mL; g/mL",
  "application_number": "BLA103753",
  "marketing_category": "BLA",
  "nonproprietary_name": "BETULA NIGRA, BETULA POPULIFOLIA",
  "start_marketing_date": "19980223",
  "active_numerator_strength": ".05; .05"
}

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