Hemlibra

UNIISPLATC B02BX06

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

Identification

ManufacturerGenentech, Inc.

CountryUS (United States)

ATC codeB02BX06

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
5024292201
1 VIAL, SINGLE-USE in 1 CARTON (50242-922-01) / .7 mL in 1 VIAL, SINGLE-USE

Annotations

UNII (FDA Substance ID)

7NL2E3F6K3

EMICIZUMAB

RxCUI 1989794

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "7NL2E3F6K3",
    "rxcui": "1989794",
    "inchikey": null,
    "display_name": "EMICIZUMAB",
    "substance_type": "protein",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "SUBCUTANEOUS",
  "spl_meta": {
    "2483adba-fab6-4d1b-96c5-c195577ed071": {
      "match": "brand_token",
      "title": "HEMLIBRA (EMICIZUMAB) INJECTION, SOLUTION [GENENTECH, INC.]",
      "spl_version": "17",
      "published_date": "2025-07-21"
    }
  },
  "productid": "50242-922_8f25ff10-e9d1-46a1-9889-e2c3f6e0d432",
  "productndc": "50242-922",
  "dosage_form": "INJECTION, SOLUTION",
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "EMICIZUMAB",
  "proprietary_name": "Hemlibra",
  "active_ingred_unit": "mg/.7mL",
  "application_number": "BLA761083",
  "marketing_category": "BLA",
  "nonproprietary_name": "emicizumab",
  "start_marketing_date": "20171116",
  "active_numerator_strength": "105"
}

Related drugs

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