PERJETA

UNIISPLATC L01FD02

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerGenentech, Inc.

CountryUS (United States)

ATC codeL01FD02

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
5024214501
1 VIAL, SINGLE-USE in 1 CARTON (50242-145-01) / 14 mL in 1 VIAL, SINGLE-USE

Annotations

UNII (FDA Substance ID)

K16AIQ8CTM

PERTUZUMAB

RxCUI 1298944

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "K16AIQ8CTM",
    "rxcui": "1298944",
    "inchikey": null,
    "display_name": "PERTUZUMAB",
    "substance_type": "protein",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRAVENOUS",
  "spl_meta": {
    "17f85d17-ab71-4f5b-9fe3-0b8c822f69ff": {
      "match": "brand_token",
      "title": "PERJETA (PERTUZUMAB) INJECTION, SOLUTION, CONCENTRATE [GENENTECH, INC.]",
      "spl_version": "27",
      "published_date": "2026-05-04"
    }
  },
  "productid": "50242-145_dfebfe9c-a0c5-41d8-bf11-ed643627e264",
  "productndc": "50242-145",
  "dosage_form": "INJECTION, SOLUTION, CONCENTRATE",
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "PERTUZUMAB",
  "proprietary_name": "PERJETA",
  "active_ingred_unit": "mg/mL",
  "application_number": "BLA125409",
  "marketing_category": "BLA",
  "nonproprietary_name": "Pertuzumab",
  "start_marketing_date": "20120608",
  "active_numerator_strength": "30"
}

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