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United States Β· US Β· US:22840-5769_36abfd47-fc5e-43c4-e063-6394a90a8731
Atlantic Cod
UNII
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerGreer Laboratories, Inc.
CountryUS (United States)
ATC codeβ
Dispensingβ
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs Β· 2
- ndc11228405769210 mL in 1 VIAL, MULTI-DOSE (22840-5769-2)
- ndc1122840576955 mL in 1 BOTTLE, DROPPER (22840-5769-5)
Annotations
UNII (FDA Substance ID)
RPX7J99EXW
ATLANTIC COD
RxCUI 900025
Raw payload (JSON)
{
"unii": {
"unii": "RPX7J99EXW",
"rxcui": "900025",
"inchikey": null,
"display_name": "ATLANTIC COD",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS",
"productid": "22840-5769_36abfd47-fc5e-43c4-e063-6394a90a8731",
"productndc": "22840-5769",
"dosage_form": "SOLUTION",
"dea_schedule": null,
"product_type": "NON-STANDARDIZED ALLERGENIC",
"substance_name": "ATLANTIC COD",
"proprietary_name": "Atlantic Cod",
"active_ingred_unit": "g/mL",
"application_number": "BLA101833",
"marketing_category": "BLA",
"nonproprietary_name": "Gadus morhua",
"start_marketing_date": "19810915",
"active_numerator_strength": ".05"
}Access this data programmatically
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