POLIVY

UNIISPLATC L01FX14

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

Identification

ManufacturerGenentech, Inc.

CountryUS (United States)

ATC codeL01FX14

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
5024210501
1 VIAL, SINGLE-DOSE in 1 CARTON (50242-105-01) / 20 mL in 1 VIAL, SINGLE-DOSE

Annotations

UNII (FDA Substance ID)

KG6VO684Z6

POLATUZUMAB VEDOTIN

RxCUI 2174090

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "KG6VO684Z6",
    "rxcui": "2174090",
    "inchikey": null,
    "display_name": "POLATUZUMAB VEDOTIN",
    "substance_type": "protein",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRAVENOUS",
  "spl_meta": {
    "20a16ab2-f338-4abb-9dcd-254bd949a2bc": {
      "match": "brand_token",
      "title": "POLIVY (POLATUZUMAB VEDOTIN) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [GENENTECH, INC.]",
      "spl_version": "14",
      "published_date": "2026-03-30"
    }
  },
  "productid": "50242-105_6e6d980b-007b-4e04-b908-dd456f137d15",
  "productndc": "50242-105",
  "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION",
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "POLATUZUMAB VEDOTIN",
  "proprietary_name": "POLIVY",
  "active_ingred_unit": "mg/7.52mL",
  "application_number": "BLA761121",
  "marketing_category": "BLA",
  "nonproprietary_name": "polatuzumab vedotin",
  "start_marketing_date": "20190610",
  "active_numerator_strength": "140"
}

Related drugs

Other records sharing ATC code L01FX14.

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