River/Red Birch Pollen

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
4964344305
5 mL in 1 VIAL, MULTI-DOSE (49643-443-05)
ndc11
4964344310
10 mL in 1 VIAL, MULTI-DOSE (49643-443-10)
ndc11
4964344330
30 mL in 1 VIAL, MULTI-DOSE (49643-443-30)
ndc11
4964344350
50 mL in 1 VIAL, MULTI-DOSE (49643-443-50)

Annotations

UNII (FDA Substance ID)

93963RFO1P

BETULA NIGRA POLLEN

RxCUI 852148

Raw payload (JSON)

{
  "unii": {
    "unii": "93963RFO1P",
    "rxcui": "852148",
    "inchikey": null,
    "display_name": "BETULA NIGRA POLLEN",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "CUTANEOUS; INTRADERMAL; SUBCUTANEOUS",
  "productid": "49643-443_36ad1e17-751d-e226-e063-6394a90ab328",
  "productndc": "49643-443",
  "dosage_form": "INJECTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "BETULA NIGRA POLLEN",
  "proprietary_name": "River/Red Birch Pollen",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA102211",
  "marketing_category": "BLA",
  "nonproprietary_name": "Betula nigra",
  "start_marketing_date": "19740312",
  "active_numerator_strength": ".05"
}

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