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United States · US · US:24208-560_f48ec619-2eda-4360-9c67-bb79bdd00353

Visudyne

Orange BookUNIISPLATC S01LA01

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

Identification

ManufacturerBausch & Lomb Incorporated
CountryUS (United States)
ATC codeS01LA01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    2420856015
    1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 CARTON (24208-560-15)

Annotations

UNII (FDA Substance ID)
0X9PA28K43
VERTEPORFIN
RxCUI 118886
Orange Book
N021119
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "0X9PA28K43",
    "rxcui": "118886",
    "inchikey": null,
    "display_name": "VERTEPORFIN",
    "substance_type": "mixture",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRAVENOUS",
  "spl_meta": {
    "952f4c80-50b1-4308-9ee6-311ffefb13df": {
      "match": "brand_token",
      "title": "VISUDYNE (VERTEPORFIN FOR INJECTION) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [BAUSCH HEALTH US LLC]",
      "spl_version": "15",
      "published_date": "2025-09-11"
    }
  },
  "productid": "24208-560_f48ec619-2eda-4360-9c67-bb79bdd00353",
  "productndc": "24208-560",
  "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION",
  "orange_book": {
    "appl_no": "021119",
    "products": [
      {
        "rs": true,
        "rld": true,
        "te_code": null,
        "strength": "15MG/VIAL",
        "product_no": "001",
        "approval_date": "Apr 12, 2000"
      }
    ],
    "appl_type": "N"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "VERTEPORFIN",
  "proprietary_name": "Visudyne",
  "active_ingred_unit": "mg/1",
  "application_number": "NDA021119",
  "marketing_category": "NDA",
  "nonproprietary_name": "verteporfin for injection",
  "start_marketing_date": "20000412",
  "active_numerator_strength": "15"
}

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