Rituxan

UNIISPLATC L01FA01

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

Identification

ManufacturerGenentech, Inc.

CountryUS (United States)

ATC codeL01FA01

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
5024205121
1 VIAL, SINGLE-USE in 1 CARTON (50242-051-21) / 10 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": "50242-051_3a716937-c2af-4bf9-976c-c34746b22ff0",
  "productndc": "50242-051",
  "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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