Lombard Poplar 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
4964339705
5 mL in 1 VIAL, MULTI-DOSE (49643-397-05)
ndc11
4964339710
10 mL in 1 VIAL, MULTI-DOSE (49643-397-10)
ndc11
4964339730
30 mL in 1 VIAL, MULTI-DOSE (49643-397-30)
ndc11
4964339750
50 mL in 1 VIAL, MULTI-DOSE (49643-397-50)

Annotations

UNII (FDA Substance ID)

0MGE63QPFJ

POPULUS NIGRA POLLEN

RxCUI 852348

Raw payload (JSON)

{
  "unii": {
    "unii": "0MGE63QPFJ",
    "rxcui": "852348",
    "inchikey": null,
    "display_name": "POPULUS NIGRA POLLEN",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "CUTANEOUS; INTRADERMAL; SUBCUTANEOUS",
  "productid": "49643-397_36ad1e17-751d-e226-e063-6394a90ab328",
  "productndc": "49643-397",
  "dosage_form": "INJECTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "POPULUS NIGRA POLLEN",
  "proprietary_name": "Lombard Poplar Pollen",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA102211",
  "marketing_category": "BLA",
  "nonproprietary_name": "Populus nigra",
  "start_marketing_date": "19740312",
  "active_numerator_strength": ".05"
}

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