Ruxience

UNIISPLATC L01FA01

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

Identification

ManufacturerPfizer Laboratories Div Pfizer Inc

CountryUS (United States)

ATC codeL01FA01

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
0069024901
1 VIAL, SINGLE-USE in 1 CARTON (0069-0249-01) / 50 mL in 1 VIAL, SINGLE-USE

Annotations

UNII (FDA Substance ID)

4F4X42SYQ6

RITUXIMAB

RxCUI 121191

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "4F4X42SYQ6",
    "rxcui": "121191",
    "inchikey": null,
    "display_name": "RITUXIMAB",
    "substance_type": "protein",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRAVENOUS",
  "spl_meta": {
    "f941fc61-f7a3-4e4a-ab7c-87c1667fa05b": {
      "match": "brand_token",
      "title": "RUXIENCE (RITUXIMAB-PVVR) INJECTION, SOLUTION [PFIZER LABORATORIES DIV PFIZER INC]",
      "spl_version": "11",
      "published_date": "2026-04-15"
    }
  },
  "productid": "0069-0249_87be604a-12ed-4b20-a7bc-8a69258abcf9",
  "productndc": "0069-0249",
  "dosage_form": "INJECTION, SOLUTION",
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "RITUXIMAB",
  "proprietary_name": "Ruxience",
  "active_ingred_unit": "mg/50mL",
  "application_number": "BLA761103",
  "marketing_category": "BLA",
  "nonproprietary_name": "rituximab-pvvr",
  "start_marketing_date": "20200123",
  "active_numerator_strength": "500"
}

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