πΊπΈ
United States Β· US Β· US:76125-900_a7b621b8-b33b-4ece-b7ba-7d63f8ec7018
GAMMAKED
UNII
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerKEDRION BIOPHARMA, INC.
CountryUS (United States)
ATC codeβ
Dispensingβ
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs Β· 5
- ndc1176125900011 VIAL, GLASS in 1 CARTON (76125-900-01) / 10 mL in 1 VIAL, GLASS (76125-900-02)
- ndc1176125900101 VIAL, GLASS in 1 CARTON (76125-900-10) / 100 mL in 1 VIAL, GLASS (76125-900-11)
- ndc1176125900201 VIAL, GLASS in 1 CARTON (76125-900-20) / 200 mL in 1 VIAL, GLASS (76125-900-21)
- ndc1176125900251 VIAL, GLASS in 1 CARTON (76125-900-25) / 25 mL in 1 VIAL, GLASS (76125-900-26)
- ndc1176125900501 VIAL, GLASS in 1 CARTON (76125-900-50) / 50 mL in 1 VIAL, GLASS (76125-900-51)
Annotations
UNII (FDA Substance ID)
66Y330CJHS
HUMAN IMMUNOGLOBULIN G
RxCUI 1426680
Raw payload (JSON)
{
"unii": {
"unii": "66Y330CJHS",
"rxcui": "1426680",
"inchikey": null,
"display_name": "HUMAN IMMUNOGLOBULIN G",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRAVENOUS; SUBCUTANEOUS",
"productid": "76125-900_a7b621b8-b33b-4ece-b7ba-7d63f8ec7018",
"productndc": "76125-900",
"dosage_form": "INJECTION",
"dea_schedule": null,
"product_type": "PLASMA DERIVATIVE",
"substance_name": "HUMAN IMMUNOGLOBULIN G",
"proprietary_name": "GAMMAKED",
"active_ingred_unit": "g/100mL",
"application_number": "BLA125046",
"marketing_category": "BLA",
"nonproprietary_name": "Immune Globulin (Human)",
"start_marketing_date": "20101013",
"active_numerator_strength": "10"
}Access this data programmatically
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