Tuna

UNII

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

Identification

ManufacturerGreer Laboratories, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 2

ndc11
2284057802
10 mL in 1 VIAL, MULTI-DOSE (22840-5780-2)
ndc11
2284057805
5 mL in 1 BOTTLE, DROPPER (22840-5780-5)

Annotations

UNII (FDA Substance ID)

12ZC3K09X7

YELLOWFIN TUNA

Raw payload (JSON)

{
  "unii": {
    "unii": "12ZC3K09X7",
    "rxcui": null,
    "inchikey": null,
    "display_name": "YELLOWFIN TUNA",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS",
  "productid": "22840-5780_36abfd47-fc5e-43c4-e063-6394a90a8731",
  "productndc": "22840-5780",
  "dosage_form": "SOLUTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "YELLOWFIN TUNA",
  "proprietary_name": "Tuna",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA101833",
  "marketing_category": "BLA",
  "nonproprietary_name": "Thunnus albacares",
  "start_marketing_date": "19810915",
  "active_numerator_strength": ".05"
}

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