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United States · US · US:50242-053_3a716937-c2af-4bf9-976c-c34746b22ff0

Rituxan

UNIISPLATC L01FA01

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

Identification

ManufacturerGenentech, Inc.
CountryUS (United States)
ATC codeL01FA01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    5024205306
    1 VIAL, SINGLE-USE in 1 CARTON (50242-053-06) / 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": {
    "3e5b7e82-f018-4eaf-ae78-d6145a906b20": {
      "match": "brand_token",
      "title": "RITUXAN HYCELA (RITUXIMAB AND HYALURONIDASE) INJECTION, SOLUTION [GENENTECH, INC.]",
      "spl_version": "21",
      "published_date": "2025-12-19"
    }
  },
  "productid": "50242-053_3a716937-c2af-4bf9-976c-c34746b22ff0",
  "productndc": "50242-053",
  "dosage_form": "INJECTION, SOLUTION",
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "RITUXIMAB",
  "proprietary_name": "Rituxan",
  "active_ingred_unit": "mg/mL",
  "application_number": "BLA103705",
  "marketing_category": "BLA",
  "nonproprietary_name": "rituximab",
  "start_marketing_date": "19971126",
  "active_numerator_strength": "10"
}

Related drugs

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