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United States · US · US:50242-260_9d068707-f189-4f0f-a74e-17bbe1f10476

Phesgo

UNIISPLATC L01FD

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerGenentech, Inc.
CountryUS (United States)
ATC codeL01FD
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 2

  • ndc11
    5024226001
    1 VIAL, SINGLE-DOSE in 1 CARTON (50242-260-01) / 10 mL in 1 VIAL, SINGLE-DOSE
  • ndc11
    5024226086
    1 VIAL, SINGLE-DOSE in 1 CARTON (50242-260-86) / 10 mL in 1 VIAL, SINGLE-DOSE

Annotations

UNII (FDA Substance ID)
743QUY4VD8
HYALURONIDASE (HUMAN RECOMBINANT)
RxCUI 1300478
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "743QUY4VD8",
    "rxcui": "1300478",
    "inchikey": null,
    "display_name": "HYALURONIDASE (HUMAN RECOMBINANT)",
    "substance_type": "protein",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "SUBCUTANEOUS",
  "spl_meta": {
    "27dd5e6b-72cd-458d-a015-cf4dab5800da": {
      "match": "brand_token",
      "title": "PHESGO (PERTUZUMAB, TRASTUZUMAB, AND HYALURONIDASE-ZZXF) INJECTION, SOLUTION [GENENTECH, INC.]",
      "spl_version": "17",
      "published_date": "2026-05-25"
    }
  },
  "productid": "50242-260_9d068707-f189-4f0f-a74e-17bbe1f10476",
  "productndc": "50242-260",
  "dosage_form": "INJECTION, SOLUTION",
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "HYALURONIDASE (HUMAN RECOMBINANT); PERTUZUMAB; TRASTUZUMAB",
  "proprietary_name": "Phesgo",
  "active_ingred_unit": "U/10mL; mg/10mL; mg/10mL",
  "application_number": "BLA761170",
  "marketing_category": "BLA",
  "nonproprietary_name": "pertuzumab, trastuzumab, and hyaluronidase-zzxf",
  "start_marketing_date": "20200629",
  "active_numerator_strength": "20000; 600; 600"
}

Related drugs

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