United States· US:76125-900_a7b621b8-b33b-4ece-b7ba-7d63f8ec7018

GAMMAKED

A medicinal product containing human immunoglobulin g, registered in United States by KEDRION BIOPHARMA, INC..

Checked against FDA National Drug Code directory (United States) on

Informational only — not a medical device.

SOURCE REGISTER · USFDA National Drug Code directory (Unite…normalisedGAMMAKEDATC—REGISTER NO.US:76125-900_a7b621b8…PACKS LISTED10CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
HUMAN IMMUNOGLOBULIN G
Manufacturer
KEDRION BIOPHARMA, INC.
Country
United States (US)
ATC code
—
Reimbursed
Not published by this register
Source register
FDA National Drug Code directory (United States)
Last checked
September 27, 2026

Packs & prices · 10

  • ndc11
    76125-900-01
  • ndc11
    76125-900-10
  • ndc11
    76125-900-20
  • 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)
  • ndc11
    76125-900-25
  • ndc11
    76125-900-50

Regulatory notes

No shortage, Orange Book or US label notes for this record.

Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of FDA National Drug Code directory (United States). This is an informational data service and not a medical device — verify against the official source of record before any clinical decision.

For developers

The same record over the API, and the raw payload
GET /v1/drugs/6c511a11-6cad-4805-bb7f-1161be06f187
GET /v1/drugs/6c511a11-6cad-4805-bb7f-1161be06f187?format=fhir

Every response carries last_synced_at, so freshness is a field rather than a promise. Below is exactly what the ingestion wrote, before any presentation — the same JSON the API returns under payload.

{
  "route": "INTRAVENOUS; SUBCUTANEOUS",
  "source": "ndc",
  "strength": "10",
  "substance": "HUMAN IMMUNOGLOBULIN G",
  "productndc": "76125-900",
  "dosage_form": "INJECTION",
  "dea_schedule": null,
  "strength_unit": "g/100mL",
  "application_number": "BLA125046",
  "marketing_category": "BLA"
}

See everything about human immunoglobulin g.

This page is the registration. A free account adds the label text as the regulator wrote it, what it costs per daily dose across the markets that publish a price, a feed of what changes in the registers, and an assistant that answers with its sources. Interaction severity is free; mechanism and management are on the Growth plan. No card, nothing to install.