Pullularia

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
4964311705
5 mL in 1 VIAL, MULTI-DOSE (49643-117-05)
ndc11
4964311710
10 mL in 1 VIAL, MULTI-DOSE (49643-117-10)
ndc11
4964311730
30 mL in 1 VIAL, MULTI-DOSE (49643-117-30)
ndc11
4964311750
50 mL in 1 VIAL, MULTI-DOSE (49643-117-50)

Annotations

UNII (FDA Substance ID)

D1A2NG69CK

AUREOBASIDIUM PULLULANS VAR. PULLUTANS

RxCUI 852102

Raw payload (JSON)

{
  "unii": {
    "unii": "D1A2NG69CK",
    "rxcui": "852102",
    "inchikey": null,
    "display_name": "AUREOBASIDIUM PULLULANS VAR. PULLUTANS",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "CUTANEOUS; INTRADERMAL; SUBCUTANEOUS",
  "productid": "49643-117_36ad1e17-751d-e226-e063-6394a90ab328",
  "productndc": "49643-117",
  "dosage_form": "INJECTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "AUREOBASIDIUM PULLULANS VAR. PULLUTANS",
  "proprietary_name": "Pullularia",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA102211",
  "marketing_category": "BLA",
  "nonproprietary_name": "Pullularia pullulans",
  "start_marketing_date": "19740312",
  "active_numerator_strength": ".01"
}

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