Alder Mix

UNII

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

Identification

ManufacturerAllermed Laboratories, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 4

ndc11
4964350105
5 mL in 1 VIAL, MULTI-DOSE (49643-501-05)
ndc11
4964350110
10 mL in 1 VIAL, MULTI-DOSE (49643-501-10)
ndc11
4964350130
30 mL in 1 VIAL, MULTI-DOSE (49643-501-30)
ndc11
4964350150
50 mL in 1 VIAL, MULTI-DOSE (49643-501-50)

Annotations

UNII (FDA Substance ID)

605T96G8Y5

ALNUS INCANA SUBSP. RUGOSA POLLEN

RxCUI 851902

Raw payload (JSON)

{
  "unii": {
    "unii": "605T96G8Y5",
    "rxcui": "851902",
    "inchikey": null,
    "display_name": "ALNUS INCANA SUBSP. RUGOSA POLLEN",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "PERCUTANEOUS; SUBCUTANEOUS",
  "productid": "49643-501_36ad277a-1b95-6b09-e063-6294a90ac5a9",
  "productndc": "49643-501",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "ALNUS INCANA SUBSP. RUGOSA POLLEN; ALNUS RHOMBIFOLIA POLLEN; ALNUS RUBRA POLLEN",
  "proprietary_name": "Alder Mix",
  "active_ingred_unit": "g/mL; g/mL; g/mL",
  "application_number": "BLA102211",
  "marketing_category": "BLA",
  "nonproprietary_name": "Alnus rhombifolia/Alnus rubra/Alnus rugosa",
  "start_marketing_date": "19740312",
  "active_numerator_strength": ".0167; .0167; .0167"
}

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