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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

  • ndc11
    7612590001
    1 VIAL, GLASS in 1 CARTON (76125-900-01) / 10 mL in 1 VIAL, GLASS (76125-900-02)
  • ndc11
    7612590010
    1 VIAL, GLASS in 1 CARTON (76125-900-10) / 100 mL in 1 VIAL, GLASS (76125-900-11)
  • ndc11
    7612590020
    1 VIAL, GLASS in 1 CARTON (76125-900-20) / 200 mL in 1 VIAL, GLASS (76125-900-21)
  • ndc11
    7612590025
    1 VIAL, GLASS in 1 CARTON (76125-900-25) / 25 mL in 1 VIAL, GLASS (76125-900-26)
  • ndc11
    7612590050
    1 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"
}

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