United States· US:57894-514_e037897a-b42a-413f-8f3f-c0f5ee7b5125
Rybrevant Faspro
A other monoclonal antibodies and antibody drug conjugates product containing amivantamab and hyaluronidase-lpuj (human recombinant), registered in United States by Janssen Biotech, Inc.. The same ATC class is registered in 5 of our 19 countries.
Checked against FDA National Drug Code directory (United States) on
Informational only — not a medical device.
Where it is registered
Amivantamab and hyaluronidase-lpuj (human recombinant) is registered in 5 of 19 countries.
Countries holding a registration under ATC L01FX (other monoclonal antibodies and antibody drug conjugates), each read from that country’s own register.
- This record: United States, from FDA National Drug Code directory (United States)
- 4 of them publish a price we can compare per daily dose
Amivantamab and hyaluronidase-lpuj (human recombinant) · ATC L01FX
5 / 19 countries
- Finlandprice
- Icelandprice
- Netherlands
- Polandprice
- United Statesprice
The record
At a glance
FDA National Drug Code directory (United States)- Active substance
- AMIVANTAMAB and HYALURONIDASE-lpuj (HUMAN RECOMBINANT)
- Manufacturer
- Janssen Biotech, Inc.
- Country
- United States (US)
- ATC code
- L01FX
- ATC class
- Other monoclonal antibodies and antibody drug conjugates
- Reimbursed
- Not published by this register
- Source register
- FDA National Drug Code directory (United States)
- Last checked
- June 3, 2026
Packs & prices · 1
- ndc1157894514011 VIAL, SINGLE-DOSE in 1 CARTON (57894-514-01) / 14 mL in 1 VIAL, SINGLE-DOSE
Regulatory notes
Same class
Other records under L01FX
Other monoclonal antibodies and antibody drug conjugates, as other registers publish it.
- NetherlandsColumvi 10 mg concentraat voor oplossing voor infusieRoche Registration GmbH
- NetherlandsColumvi 2,5 mg concentraat voor oplossing voor infusieRoche Registration GmbH
- PolandDatrowayDaiichi Sankyo Europe GmbH
- PolandElrexfioPfizer Europe MA EEIG
- PolandIMDYLLTRAAmgen Europe B.V.
- PolandIMDYLLTRAAmgen Europe B.V.
- IcelandLynozyficRegeneron Ireland Designated Activity Company
- IcelandLynozyficRegeneron Ireland Designated Activity Company
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/f549f8d9-9cd9-4862-8168-6ecd475bc5bc GET /v1/drugs/f549f8d9-9cd9-4862-8168-6ecd475bc5bc?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.
{
"unii": {
"unii": "0JSR7Z0NB6",
"rxcui": "2549199",
"inchikey": null,
"display_name": "AMIVANTAMAB",
"substance_type": "protein",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "SUBCUTANEOUS",
"spl_meta": {
"1466c070-9f97-4fa4-a955-6a6b59981fb8": {
"match": "brand_token",
"title": "RYBREVANT (AMIVANTAMAB-VMJW) INJECTION [JANSSEN BIOTECH, INC.]",
"spl_version": "16",
"published_date": "2026-03-18"
}
},
"productid": "57894-514_e037897a-b42a-413f-8f3f-c0f5ee7b5125",
"productndc": "57894-514",
"dosage_form": "INJECTION",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "AMIVANTAMAB; HYALURONIDASE (HUMAN RECOMBINANT)",
"proprietary_name": "Rybrevant Faspro",
"active_ingred_unit": "mg/14mL; mg/14mL",
"application_number": "BLA761433",
"marketing_category": "BLA",
"nonproprietary_name": "AMIVANTAMAB and HYALURONIDASE-lpuj (HUMAN RECOMBINANT)",
"start_marketing_date": "20251219",
"active_numerator_strength": "2240; 28000"
}See everything about amivantamab and hyaluronidase-lpuj (human recombinant).
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.