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United States · US · US:49643-109_36ad1e17-751d-e226-e063-6394a90ab328

Curvularia

UNII

Last synced from FDA National Drug Code directory (United States) on

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
    4964310905
    5 mL in 1 VIAL, MULTI-DOSE (49643-109-05)
  • ndc11
    4964310910
    10 mL in 1 VIAL, MULTI-DOSE (49643-109-10)
  • ndc11
    4964310930
    30 mL in 1 VIAL, MULTI-DOSE (49643-109-30)
  • ndc11
    4964310950
    50 mL in 1 VIAL, MULTI-DOSE (49643-109-50)

Annotations

UNII (FDA Substance ID)
4T82EA86AJ
COCHLIOBOLUS LUNATUS
Raw payload (JSON)
{
  "unii": {
    "unii": "4T82EA86AJ",
    "rxcui": null,
    "inchikey": null,
    "display_name": "COCHLIOBOLUS LUNATUS",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "CUTANEOUS; INTRADERMAL; SUBCUTANEOUS",
  "productid": "49643-109_36ad1e17-751d-e226-e063-6394a90ab328",
  "productndc": "49643-109",
  "dosage_form": "INJECTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "COCHLIOBOLUS LUNATUS",
  "proprietary_name": "Curvularia",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA102211",
  "marketing_category": "BLA",
  "nonproprietary_name": "Curvularia lunata",
  "start_marketing_date": "19740312",
  "active_numerator_strength": ".1"
}

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