Oyster

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
2284057742
10 mL in 1 VIAL, MULTI-DOSE (22840-5774-2)
ndc11
2284057745
5 mL in 1 BOTTLE, DROPPER (22840-5774-5)

Annotations

UNII (FDA Substance ID)

0I77C68AWS

EASTERN OYSTER

Raw payload (JSON)

{
  "unii": {
    "unii": "0I77C68AWS",
    "rxcui": null,
    "inchikey": null,
    "display_name": "EASTERN OYSTER",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS",
  "productid": "22840-5774_36abfd47-fc5e-43c4-e063-6394a90a8731",
  "productndc": "22840-5774",
  "dosage_form": "SOLUTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "EASTERN OYSTER",
  "proprietary_name": "Oyster",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA101833",
  "marketing_category": "BLA",
  "nonproprietary_name": "Crassostrea virginica",
  "start_marketing_date": "19810915",
  "active_numerator_strength": ".05"
}

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